RAB29 c.*204G>A

Variant ID: 1-205739266-C-T

NM_003929.2(RAB29):c.*204G>A

This variant was identified in 24 publications

View GRCh38 version.




Publications:


Brain expression quantitative trait locus and network analyses reveal downstream effects and putative drivers for brain-related diseases.

Nature Genetics
de Klein, Niek N; Tsai, Ellen A EA; Vochteloo, Martijn M; Baird, Denis D; Huang, Yunfeng Y; Chen, Chia-Yen CY; van Dam, Sipko S; Oelen, Roy R; Deelen, Patrick P; Bakker, Olivier B OB; El Garwany, Omar O; Ouyang, Zhengyu Z; Marshall, Eric E EE; Zavodszky, Maria I MI; van Rheenen, Wouter W; Bakker, Mark K MK; Veldink, Jan J; Gaunt, Tom R TR; Runz, Heiko H; Franke, Lude L; Westra, Harm-Jan HJ
Publication Date: 2023-02-23

Variant appearance in text: rs708723
PubMed Link: 36823318
Variant Present in the following documents:
  • Main text
  • 41588_2023_Article_1300.pdf
View BVdb publication page



Genetic overlap between Parkinson's disease and inflammatory bowel disease.

Brain Communications
Kang, Xiaoying X; Ploner, Alexander A; Wang, Yunzhang Y; Ludvigsson, Jonas F JF; Williams, Dylan M DM; Pedersen, Nancy L NL; Wirdefeldt, Karin K
Publication Date: 2023

Variant appearance in text: rs708723
PubMed Link: 36687396
Variant Present in the following documents:
  • Main text
  • fcad002.pdf
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs708723
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs708723
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs708723
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.

Prostate Cancer And Prostatic Diseases
Huynh-Le, Minh-Phuong MP; Karunamuni, Roshan R; Fan, Chun Chieh CC; Asona, Lui L; Thompson, Wesley K WK; Martinez, Maria Elena ME; Eeles, Rosalind A RA; Kote-Jarai, Zsofia Z; Muir, Kenneth R KR; Lophatananon, Artitaya A; Schleutker, Johanna J; Pashayan, Nora N; Batra, Jyotsna J; Grönberg, Henrik H; Neal, David E DE; Nordestgaard, Børge G BG; Tangen, Catherine M CM; MacInnis, Robert J RJ; Wolk, Alicja A; Albanes, Demetrius D; Haiman, Christopher A CA; Travis, Ruth C RC; Blot, William J WJ; Stanford, Janet L JL; Mucci, Lorelei A LA; West, Catharine M L CML; Nielsen, Sune F SF; Kibel, Adam S AS; Cussenot, Olivier O; Berndt, Sonja I SI; Koutros, Stella S; Sørensen, Karina Dalsgaard KD; Cybulski, Cezary C; Grindedal, Eli Marie EM; Menegaux, Florence F; Park, Jong Y JY; Ingles, Sue A SA; Maier, Christiane C; Hamilton, Robert J RJ; Rosenstein, Barry S BS; Lu, Yong-Jie YJ; Watya, Stephen S; Vega, Ana A; Kogevinas, Manolis M; Wiklund, Fredrik F; Penney, Kathryn L KL; Huff, Chad D CD; Teixeira, Manuel R MR; Multigner, Luc L; Leach, Robin J RJ; Brenner, Hermann H; John, Esther M EM; Kaneva, Radka R; Logothetis, Christopher J CJ; Neuhausen, Susan L SL; De Ruyck, Kim K; Ost, Piet P; Razack, Azad A; Newcomb, Lisa F LF; Fowke, Jay H JH; Gamulin, Marija M; Abraham, Aswin A; Claessens, Frank F; Castelao, Jose Esteban JE; Townsend, Paul A PA; Crawford, Dana C DC; Petrovics, Gyorgy G; van Schaik, Ron H N RHN; Parent, Marie-Élise MÉ; Hu, Jennifer J JJ; Zheng, Wei W; , ; , ; , ; , ; , ; , ; , ; Mills, Ian G IG; Andreassen, Ole A OA; Dale, Anders M AM; Seibert, Tyler M TM
Publication Date: 2022-04

Variant appearance in text: rs708723
PubMed Link: 35152271
Variant Present in the following documents:
  • 41391_2022_497_MOESM1_ESM.pdf
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Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs708723
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Genetic and Environmental Factors Influence the Pleomorphy of LRRK2 Parkinsonism.

International Journal Of Molecular Sciences
Chittoor-Vinod, Vinita G VG; Nichols, R Jeremy RJ; Schüle, Birgitt B
Publication Date: 2021-01-21

Variant appearance in text: rs708723
PubMed Link: 33494262
Variant Present in the following documents:
  • Main text
View BVdb publication page



Allele-specific expression of Parkinson's disease susceptibility genes in human brain.

Scientific Reports
Langmyhr, Margrete M; Henriksen, Sandra Pilar SP; Cappelletti, Chiara C; van de Berg, Wilma D J WDJ; Pihlstrøm, Lasse L; Toft, Mathias M
Publication Date: 2021-01-12

Variant appearance in text: rs708723
PubMed Link: 33436766
Variant Present in the following documents:
  • Main text
  • 41598_2020_79990_MOESM1_ESM.pdf
  • 41598_2020_Article_79990.pdf
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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: rs708723
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

Nature Communications
Dadaev, Tokhir T; Saunders, Edward J EJ; Newcombe, Paul J PJ; Anokian, Ezequiel E; Leongamornlert, Daniel A DA; Brook, Mark N MN; Cieza-Borrella, Clara C; Mijuskovic, Martina M; Wakerell, Sarah S; Olama, Ali Amin Al AAA; Schumacher, Fredrick R FR; Berndt, Sonja I SI; Benlloch, Sara S; Ahmed, Mahbubl M; Goh, Chee C; Sheng, Xin X; Zhang, Zhuo Z; Muir, Kenneth K; Govindasami, Koveela K; Lophatananon, Artitaya A; Stevens, Victoria L VL; Gapstur, Susan M SM; Carter, Brian D BD; Tangen, Catherine M CM; Goodman, Phyllis P; Thompson, Ian M IM; Batra, Jyotsna J; Chambers, Suzanne S; Moya, Leire L; Clements, Judith J; Horvath, Lisa L; Tilley, Wayne W; Risbridger, Gail G; Gronberg, Henrik H; Aly, Markus M; Nordström, Tobias T; Pharoah, Paul P; Pashayan, Nora N; Schleutker, Johanna J; Tammela, Teuvo L J TLJ; Sipeky, Csilla C; Auvinen, Anssi A; Albanes, Demetrius D; Weinstein, Stephanie S; Wolk, Alicja A; Hakansson, Niclas N; West, Catharine C; Dunning, Alison M AM; Burnet, Neil N; Mucci, Lorelei L; Giovannucci, Edward E; Andriole, Gerald G; Cussenot, Olivier O; Cancel-Tassin, Géraldine G; Koutros, Stella S; Freeman, Laura E Beane LEB; Sorensen, Karina Dalsgaard KD; Orntoft, Torben Falck TF; Borre, Michael M; Maehle, Lovise L; Grindedal, Eli Marie EM; Neal, David E DE; Donovan, Jenny L JL; Hamdy, Freddie C FC; Martin, Richard M RM; Travis, Ruth C RC; Key, Tim J TJ; Hamilton, Robert J RJ; Fleshner, Neil E NE; Finelli, Antonio A; Ingles, Sue Ann SA; Stern, Mariana C MC; Rosenstein, Barry B; Kerns, Sarah S; Ostrer, Harry H; Lu, Yong-Jie YJ; Zhang, Hong-Wei HW; Feng, Ninghan N; Mao, Xueying X; Guo, Xin X; Wang, Guomin G; Sun, Zan Z; Giles, Graham G GG; Southey, Melissa C MC; MacInnis, Robert J RJ; FitzGerald, Liesel M LM; Kibel, Adam S AS; Drake, Bettina F BF; Vega, Ana A; Gómez-Caamaño, Antonio A; Fachal, Laura L; Szulkin, Robert R; Eklund, Martin M; Kogevinas, Manolis M; Llorca, Javier J; Castaño-Vinyals, Gemma G; Penney, Kathryn L KL; Stampfer, Meir M; Park, Jong Y JY; Sellers, Thomas A TA; Lin, Hui-Yi HY; Stanford, Janet L JL; Cybulski, Cezary C; Wokolorczyk, Dominika D; Lubinski, Jan J; Ostrander, Elaine A EA; Geybels, Milan S MS; Nordestgaard, Børge G BG; Nielsen, Sune F SF; Weisher, Maren M; Bisbjerg, Rasmus R; Røder, Martin Andreas MA; Iversen, Peter P; Brenner, Hermann H; Cuk, Katarina K; Holleczek, Bernd B; Maier, Christiane C; Luedeke, Manuel M; Schnoeller, Thomas T; Kim, Jeri J; Logothetis, Christopher J CJ; John, Esther M EM; Teixeira, Manuel R MR; Paulo, Paula P; Cardoso, Marta M; Neuhausen, Susan L SL; Steele, Linda L; Ding, Yuan Chun YC; De Ruyck, Kim K; De Meerleer, Gert G; Ost, Piet P; Razack, Azad A; Lim, Jasmine J; Teo, Soo-Hwang SH; Lin, Daniel W DW; Newcomb, Lisa F LF; Lessel, Davor D; Gamulin, Marija M; Kulis, Tomislav T; Kaneva, Radka R; Usmani, Nawaid N; Slavov, Chavdar C; Mitev, Vanio V; Parliament, Matthew M; Singhal, Sandeep S; Claessens, Frank F; Joniau, Steven S; Van den Broeck, Thomas T; Larkin, Samantha S; Townsend, Paul A PA; Aukim-Hastie, Claire C; Gago-Dominguez, Manuela M; Castelao, Jose Esteban JE; Martinez, Maria Elena ME; Roobol, Monique J MJ; Jenster, Guido G; van Schaik, Ron H N RHN; Menegaux, Florence F; Truong, Thérèse T; Koudou, Yves Akoli YA; Xu, Jianfeng J; Khaw, Kay-Tee KT; Cannon-Albright, Lisa L; Pandha, Hardev H; Michael, Agnieszka A; Kierzek, Andrzej A; Thibodeau, Stephen N SN; McDonnell, Shannon K SK; Schaid, Daniel J DJ; Lindstrom, Sara S; Turman, Constance C; Ma, Jing J; Hunter, David J DJ; Riboli, Elio E; Siddiq, Afshan A; Canzian, Federico F; Kolonel, Laurence N LN; Le Marchand, Loic L; Hoover, Robert N RN; Machiela, Mitchell J MJ; Kraft, Peter P; , ; Freedman, Matthew M; Wiklund, Fredrik F; Chanock, Stephen S; Henderson, Brian E BE; Easton, Douglas F DF; Haiman, Christopher A CA; Eeles, Rosalind A RA; Conti, David V DV; Kote-Jarai, Zsofia Z
Publication Date: 2018-06-11

Variant appearance in text: rs708723
PubMed Link: 29892050
Variant Present in the following documents:
  • 41467_2018_4109_MOESM4_ESM.xlsx, sheet 3
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs708723
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs708723
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD).

Frontiers In Molecular Neuroscience
Ritter, McKenzie L ML; Guo, Wei W; Samuels, Jack F JF; Wang, Ying Y; Nestadt, Paul S PS; Krasnow, Janice J; Greenberg, Benjamin D BD; Fyer, Abby J AJ; McCracken, James T JT; Geller, Daniel A DA; Murphy, Dennis L DL; Knowles, James A JA; Grados, Marco A MA; Riddle, Mark A MA; Rasmussen, Steven A SA; McLaughlin, Nicole C NC; Nurmi, Erika L EL; Askland, Kathleen D KD; Cullen, Bernadette B; Piacentini, John J; Pauls, David L DL; Bienvenu, Joseph J; Stewart, Evelyn E; Goes, Fernando S FS; Maher, Brion B; Pulver, Ann E AE; Mattheisen, Manuel M; Qian, Ji J; Nestadt, Gerald G; Shugart, Yin Yao YY
Publication Date: 2017

Variant appearance in text: rs708723
PubMed Link: 28386217
Variant Present in the following documents:
  • Main text
  • fnmol-10-00083.pdf
View BVdb publication page



Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study.

Neurobiology Of Aging
Wang, Lisa L; Heckman, Michael G MG; Aasly, Jan O JO; Annesi, Grazia G; Bozi, Maria M; Chung, Sun Ju SJ; Clarke, Carl C; Crosiers, David D; Eckstein, Gertrud G; Garraux, Gaetan G; Hadjigeorgiou, Georgios M GM; Hattori, Nobu N; Jeon, Beom B; Kim, Yun J YJ; Kubo, Masato M; Lesage, Suzanne S; Lin, Juei Jueng JJ; Lynch, Timothy T; Lichtner, Peter P; Mellick, George D GD; Mok, Vincent V; Morrison, Karin E KE; Quattrone, Aldo A; Satake, Wataru W; Silburn, Peter A PA; Stefanis, Leonidas L; Stockton, Joanne D JD; Tan, Eng King EK; Toda, Tatsushi T; Brice, Alexis A; Van Broeckhoven, Christine C; Uitti, Ryan J RJ; Wirdefeldt, Karin K; Wszolek, Zbigniew Z; Xiromerisiou, Georgia G; Maraganore, Demetrius M DM; Gasser, Thomas T; Krüger, Rejko R; Farrer, Matthew J MJ; Ross, Owen A OA; Sharma, Manu M; ,
Publication Date: 2017-01

Variant appearance in text: rs708723
PubMed Link: 27814993
Variant Present in the following documents:
  • Main text
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs708723
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 3
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs708723
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease.

Proceedings Of The National Academy Of Sciences Of The United States Of America
Beilina, Alexandria A; Rudenko, Iakov N IN; Kaganovich, Alice A; Civiero, Laura L; Chau, Hien H; Kalia, Suneil K SK; Kalia, Lorraine V LV; Lobbestael, Evy E; Chia, Ruth R; Ndukwe, Kelechi K; Ding, Jinhui J; Nalls, Mike A MA; , ; , ; Olszewski, Maciej M; Hauser, David N DN; Kumaran, Ravindran R; Lozano, Andres M AM; Baekelandt, Veerle V; Greene, Lois E LE; Taymans, Jean-Marc JM; Greggio, Elisa E; Cookson, Mark R MR
Publication Date: 2014-02-18

Variant appearance in text: rs708723
PubMed Link: 24510904
Variant Present in the following documents:
  • Main text
View BVdb publication page



GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.

American Journal Of Neurodegenerative Disease
Soto-Ortolaza, Alexandra I AI; Heckman, Michael G MG; Labbé, Catherine C; Serie, Daniel J DJ; Puschmann, Andreas A; Rayaprolu, Sruti S; Strongosky, Audrey A; Boczarska-Jedynak, Magdalena M; Opala, Grzegorz G; Krygowska-Wajs, Anna A; Barcikowska, Maria M; Czyzewski, Krzysztof K; Lynch, Timothy T; Uitti, Ryan J RJ; Wszolek, Zbigniew K ZK; Ross, Owen A OA
Publication Date: 2013

Variant appearance in text: rs708723
PubMed Link: 24319646
Variant Present in the following documents:
  • Main text
View BVdb publication page



Assessment of Parkinson's disease risk loci in Greece.

Neurobiology Of Aging
Kara, Eleanna E; Xiromerisiou, Georgia G; Spanaki, Cleanthe C; Bozi, Maria M; Koutsis, Georgios G; Panas, Marios M; Dardiotis, Efthimios E; Ralli, Styliani S; Bras, Jose J; Letson, Christopher C; Edsall, Connor C; Pliner, Hannah H; Arepalli, Sampath S; Kalinderi, Kallirhoe K; Fidani, Liana L; Bostantjopoulou, Sevasti S; Keller, Margaux F MF; Wood, Nicholas W NW; Hardy, John J; Houlden, Henry H; Stefanis, Leonidas L; Plaitakis, Andreas A; Hernandez, Dena D; Hadjigeorgiou, Georgios M GM; Nalls, Mike A MA; Singleton, Andrew B AB
Publication Date: 2014-02

Variant appearance in text: rs708723
PubMed Link: 24080174
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome wide assessment of young onset Parkinson's disease from Finland.

Plos One
Hernandez, Dena G DG; Nalls, Michael A MA; Ylikotila, Pauli P; Keller, Margaux M; Hardy, John A JA; Majamaa, Kari K; Singleton, Andrew B AB
Publication Date: 2012

Variant appearance in text: rs708723
PubMed Link: 22911860
Variant Present in the following documents:
  • Main text
  • pone.0041859.pdf
View BVdb publication page



Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.

Human Molecular Genetics
Keller, Margaux F MF; Saad, Mohamad M; Bras, Jose J; Bettella, Francesco F; Nicolaou, Nayia N; Simón-Sánchez, Javier J; Mittag, Florian F; Büchel, Finja F; Sharma, Manu M; Gibbs, J Raphael JR; Schulte, Claudia C; Moskvina, Valentina V; Durr, Alexandra A; Holmans, Peter P; Kilarski, Laura L LL; Guerreiro, Rita R; Hernandez, Dena G DG; Brice, Alexis A; Ylikotila, Pauli P; Stefánsson, Hreinn H; Majamaa, Kari K; Morris, Huw R HR; Williams, Nigel N; Gasser, Thomas T; Heutink, Peter P; Wood, Nicholas W NW; Hardy, John J; Martinez, Maria M; Singleton, Andrew B AB; Nalls, Michael A MA; , ; ,
Publication Date: 2012-11-15

Variant appearance in text: rs708723
PubMed Link: 22892372
Variant Present in the following documents:
  • Main text
View BVdb publication page



No association between Parkinson disease alleles and the risk of melanoma.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Meng, Shasha S; Song, Fengju F; Chen, Honglei H; Gao, Xiang X; Amos, Christopher I CI; Lee, Jeffrey E JE; Wei, Qingyi Q; Qureshi, Abrar A AA; Han, Jiali J
Publication Date: 2012-01

Variant appearance in text: rs708723
PubMed Link: 22086882
Variant Present in the following documents:
  • Main text
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A two-stage meta-analysis identifies several new loci for Parkinson's disease.

Plos Genetics
, ; ,
Publication Date: 2011-06

Variant appearance in text: rs708723
PubMed Link: 21738488
Variant Present in the following documents:
  • Main text
  • pgen.1002142.pdf
View BVdb publication page