SKIV2L c.452A>G ;(p.Q151R)

Variant ID: 6-31928306-A-G

NM_006929.4(SKIV2L):c.452A>G;(p.Q151R)

This variant was identified in 32 publications

View GRCh38 version.




Publications:


Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs438999
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Proteomic genotyping of SNP of Complement Factor H (CFH) Y402H and I62V using multiple reaction monitoring (MRM) assays.

Scientific Reports
Kim, Kyoung Lae KL; Kim, Hyerim H; Lee, Youngju Y; Lee, Cheolju C; Joo, Kwangsic K; Park, Sang Jun SJ; Park, Kyu Hyung KH; Park, Seong-Jun SJ; Woo, Se Joon SJ
Publication Date: 2022-11-15

Variant appearance in text: rs438999
PubMed Link: 36379987
Variant Present in the following documents:
  • 41598_2022_Article_20936.pdf
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: SKIV2L: Q151R
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM9_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM13_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: SKIV2L: Q151R
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



Bacillus Calmette-Guérin Treatment Changes the Tumor Microenvironment of Non-Muscle-Invasive Bladder Cancer.

Frontiers In Oncology
Su, Fei F; Liu, Ming M; Zhang, Wei W; Tang, Min M; Zhang, Jinsong J; Li, Hexin H; Zou, Lihui L; Zhang, Rui R; Liu, Yudong Y; Li, Lin L; Ma, Jie J; Zhang, Yaqun Y; Chen, Meng M; Xiao, Fei F
Publication Date: 2022

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 35311085
Variant Present in the following documents:
  • Table_1.xlsx, sheet 4
View BVdb publication page



Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders.

Nature Neuroscience
Yang, Chengran C; Farias, Fabiana H G FHG; Ibanez, Laura L; Suhy, Adam A; Sadler, Brooke B; Fernandez, Maria Victoria MV; Wang, Fengxian F; Bradley, Joseph L JL; Eiffert, Brett B; Bahena, Jorge A JA; Budde, John P JP; Li, Zeran Z; Dube, Umber U; Sung, Yun Ju YJ; Mihindukulasuriya, Kathie A KA; Morris, John C JC; Fagan, Anne M AM; Perrin, Richard J RJ; Benitez, Bruno A BA; Rhinn, Herve H; Harari, Oscar O; Cruchaga, Carlos C
Publication Date: 2021-09

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 34239129
Variant Present in the following documents:
  • NIHMS1711548-supplement-supTables1to35.xlsx, sheet 4
View BVdb publication page



Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders.

Nature Neuroscience
Yang, Chengran C; Farias, Fabiana H G FHG; Ibanez, Laura L; Suhy, Adam A; Sadler, Brooke B; Fernandez, Maria Victoria MV; Wang, Fengxian F; Bradley, Joseph L JL; Eiffert, Brett B; Bahena, Jorge A JA; Budde, John P JP; Li, Zeran Z; Dube, Umber U; Sung, Yun Ju YJ; Mihindukulasuriya, Kathie A KA; Morris, John C JC; Fagan, Anne M AM; Perrin, Richard J RJ; Benitez, Bruno A BA; Rhinn, Herve H; Harari, Oscar O; Cruchaga, Carlos C
Publication Date: 2021-09

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 34239129
Variant Present in the following documents:
  • NIHMS1711548-supplement-supTables1to35.xlsx, sheet 4
View BVdb publication page



Steroid 21-hydroxylase gene variants and late-life depression.

Bmc Research Notes
Ancelin, Marie-Laure ML; Norton, Joanna J; Ritchie, Karen K; Chaudieu, Isabelle I; Ryan, Joanne J
Publication Date: 2021-05-25

Variant appearance in text: rs438999
PubMed Link: 34034803
Variant Present in the following documents:
  • Main text
  • 13104_2021_Article_5616.pdf
View BVdb publication page



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: SKIV2L: Q151R; rs438999
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



The Biological Significance of Multi-copy Regions and Their Impact on Variant Discovery.

Genomics, Proteomics & Bioinformatics
Sun, Jing J; Zhang, Yanfang Y; Wang, Minhui M; Guan, Qian Q; Yang, Xiujia X; Ou, Jin Xia JX; Yan, Mingchen M; Wang, Chengrui C; Zhang, Yan Y; Li, Zhi-Hao ZH; Lan, Chunhong C; Mao, Chen C; Zhou, Hong-Wei HW; Hao, Bingtao B; Zhang, Zhenhai Z
Publication Date: 2020-10

Variant appearance in text: SKIV2L: 452A>G; Gln151Arg
PubMed Link: 32827758
Variant Present in the following documents:
  • mmc12.xlsx, sheet 1
View BVdb publication page



Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.

Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 32273506
Variant Present in the following documents:
  • 41467_2020_15456_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



The role of myoglobin in epithelial cancers: Insights from transcriptomics.

International Journal Of Molecular Medicine
Bicker, Anne A; Nauth, Theresa T; Gerst, Daniela D; Aboouf, Mostafa Ahmed MA; Fandrey, Joachim J; Kristiansen, Glen G; Gorr, Thomas Alexander TA; Hankeln, Thomas T
Publication Date: 2020-02

Variant appearance in text: SKIV2L: 452A>G; Gln151Arg
PubMed Link: 31894249
Variant Present in the following documents:
  • Supplementary_Data2.xlsx, sheet 3
  • Supplementary_Data2.xlsx, sheet 4
  • Supplementary_Data2.xlsx, sheet 2
  • Supplementary_Data2.xlsx, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: SKIV2L: 452A>G; Gln151Arg; rs438999
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



An RNA Metabolism and Surveillance Quartet in the Major Histocompatibility Complex.

Cells
Zhou, Danlei D; Lai, Michalea M; Luo, Aiqin A; Yu, Chack-Yung CY
Publication Date: 2019-08-30

Variant appearance in text: rs438999
PubMed Link: 31480283
Variant Present in the following documents:
  • Main text
  • cells-08-01008.pdf
View BVdb publication page



An enhanced workflow for variant interpretation in UniProtKB/Swiss-Prot improves consistency and reuse in ClinVar.

Database : The Journal Of Biological Databases And Curation
Famiglietti, M L ML; Estreicher, A A; Breuza, L L; Poux, S S; Redaschi, N N; Xenarios, I I; Bridge, A A; ,
Publication Date: 2019-01-01

Variant appearance in text: SKIV2L: 452A>G; Gln151Arg
PubMed Link: 30937429
Variant Present in the following documents:
  • famiglietti_supplementarytables1_rev_baz040.xlsx, sheet 1
View BVdb publication page



Genetic risk factors for late age-related macular degeneration in India.

The British Journal Of Ophthalmology
Rajendran, Anand A; Dhoble, Pankaja P; Sundaresan, Periasamy P; Saravanan, Vijayan V; Vashist, Praveen P; Nitsch, Dorothea D; Smeeth, Liam L; Chakravarthy, Usha U; Ravindran, Ravilla D RD; Fletcher, Astrid E AE
Publication Date: 2018-09

Variant appearance in text: rs438999
PubMed Link: 29259020
Variant Present in the following documents:
  • Main text
  • bjophthalmol-2017-311384.pdf
View BVdb publication page



Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus.

Plos One
Rosenberger, Albert A; Sohns, Melanie M; Friedrichs, Stefanie S; Hung, Rayjean J RJ; Fehringer, Gord G; McLaughlin, John J; Amos, Christopher I CI; Brennan, Paul P; Risch, Angela A; Brüske, Irene I; Caporaso, Neil E NE; Landi, Maria Teresa MT; Christiani, David C DC; Wei, Yongyue Y; Bickeböller, Heike H
Publication Date: 2017

Variant appearance in text: rs438999
PubMed Link: 28273134
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis.

Arthritis & Rheumatology (Hoboken, N.J.)
Merkel, Peter A PA; Xie, Gang G; Monach, Paul A PA; Ji, Xuemei X; Ciavatta, Dominic J DJ; Byun, Jinyoung J; Pinder, Benjamin D BD; Zhao, Ai A; Zhang, Jinyi J; Tadesse, Yohannes Y; Qian, David D; Weirauch, Matthew M; Nair, Rajan R; Tsoi, Alex A; Pagnoux, Christian C; Carette, Simon S; Chung, Sharon S; Cuthbertson, David D; Davis, John C JC; Dellaripa, Paul F PF; Forbess, Lindsy L; Gewurz-Singer, Ora O; Hoffman, Gary S GS; Khalidi, Nader N; Koening, Curry C; Langford, Carol A CA; Mahr, Alfred D AD; McAlear, Carol C; Moreland, Larry L; Seo, E Philip EP; Specks, Ulrich U; Spiera, Robert F RF; Sreih, Antoine A; St Clair, E William EW; Stone, John H JH; Ytterberg, Steven R SR; Elder, James T JT; Qu, Jia J; Ochi, Toshiki T; Hirano, Naoto N; Edberg, Jeffrey C JC; Falk, Ronald J RJ; Amos, Christopher I CI; Siminovitch, Katherine A KA; ,
Publication Date: 2017-05

Variant appearance in text: rs438999
PubMed Link: 28029757
Variant Present in the following documents:
  • ART-69-1054-s002.pdf
View BVdb publication page



Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

The Journal Of Pathology
Maguire, Sarah L SL; Peck, Barrie B; Wai, Patty T PT; Campbell, James J; Barker, Holly H; Gulati, Aditi A; Daley, Frances F; Vyse, Simon S; Huang, Paul P; Lord, Christopher J CJ; Farnie, Gillian G; Brennan, Keith K; Natrajan, Rachael R
Publication Date: 2016-11

Variant appearance in text: SKIV2L: Q151R; rs438999
PubMed Link: 27512948
Variant Present in the following documents:
  • PATH-240-315-s015.xlsx, sheet 1
View BVdb publication page



Impact of polymorphisms in microRNA biogenesis genes on colon cancer risk and microRNA expression levels: a population-based, case-control study.

Bmc Medical Genomics
Mullany, Lila E LE; Herrick, Jennifer S JS; Wolff, Roger K RK; Buas, Matthew F MF; Slattery, Martha L ML
Publication Date: 2016-04-23

Variant appearance in text: rs438999
PubMed Link: 27107574
Variant Present in the following documents:
  • Main text
  • 12920_2016_Article_181.pdf
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs438999
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 3
View BVdb publication page



Clinical and genetic factors associated with progression of geographic atrophy lesions in age-related macular degeneration.

Plos One
Grassmann, Felix F; Fleckenstein, Monika M; Chew, Emily Y EY; Strunz, Tobias T; Schmitz-Valckenberg, Steffen S; Göbel, Arno P AP; Klein, Michael L ML; Ratnapriya, Rinki R; Swaroop, Anand A; Holz, Frank G FG; Weber, Bernhard H F BH
Publication Date: 2015

Variant appearance in text: rs438999
PubMed Link: 25962167
Variant Present in the following documents:
  • Main text
  • pone.0126636.pdf
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: SKIV2L: Q151R; rs438999
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: SKIV2L: Q151R; rs438999
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis.

Plos One
Patiño, Liliana Catherine LC; Battu, Rajani R; Ortega-Recalde, Oscar O; Nallathambi, Jeyabalan J; Anandula, Venkata Ramana VR; Renukaradhya, Umashankar U; Laissue, Paul P
Publication Date: 2014

Variant appearance in text: SKIV2L: Q151R
PubMed Link: 25333361
Variant Present in the following documents:
  • pone.0109576.s001.xls, sheet 3
  • pone.0109576.s003.xls, sheet 3
View BVdb publication page



Host genetics and immune control of HIV-1 infection: fine mapping for the extended human MHC region in an African cohort.

Genes And Immunity
Prentice, H A HA; Pajewski, N M NM; He, D D; Zhang, K K; Brown, E E EE; Kilembe, W W; Allen, S S; Hunter, E E; Kaslow, R A RA; Tang, J J
Publication Date: 2014

Variant appearance in text: SKIV2L: Q151R; rs438999
PubMed Link: 24784026
Variant Present in the following documents:
  • NIHMS580846-supplement-1.xlsx, sheet 2
  • NIHMS580846-supplement-1.xlsx, sheet 3
View BVdb publication page



Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.

Nature Genetics
Zhan, Xiaowei X; Larson, David E DE; Wang, Chaolong C; Koboldt, Daniel C DC; Sergeev, Yuri V YV; Fulton, Robert S RS; Fulton, Lucinda L LL; Fronick, Catrina C CC; Branham, Kari E KE; Bragg-Gresham, Jennifer J; Jun, Goo G; Hu, Youna Y; Kang, Hyun Min HM; Liu, Dajiang D; Othman, Mohammad M; Brooks, Matthew M; Ratnapriya, Rinki R; Boleda, Alexis A; Grassmann, Felix F; von Strachwitz, Claudia C; Olson, Lana M LM; Buitendijk, Gabriëlle H S GH; Hofman, Albert A; van Duijn, Cornelia M CM; Cipriani, Valentina V; Moore, Anthony T AT; Shahid, Humma H; Jiang, Yingda Y; Conley, Yvette P YP; Morgan, Denise J DJ; Kim, Ivana K IK; Johnson, Matthew P MP; Cantsilieris, Stuart S; Richardson, Andrea J AJ; Guymer, Robyn H RH; Luo, Hongrong H; Ouyang, Hong H; Licht, Christoph C; Pluthero, Fred G FG; Zhang, Mindy M MM; Zhang, Kang K; Baird, Paul N PN; Blangero, John J; Klein, Michael L ML; Farrer, Lindsay A LA; DeAngelis, Margaret M MM; Weeks, Daniel E DE; Gorin, Michael B MB; Yates, John R W JR; Klaver, Caroline C W CC; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Weber, Bernhard H F BH; Wilson, Richard K RK; Heckenlively, John R JR; Chew, Emily Y EY; Stambolian, Dwight D; Mardis, Elaine R ER; Swaroop, Anand A; Abecasis, Goncalo R GR
Publication Date: 2013-11

Variant appearance in text: SKIV2L: Q151R; rs438999
PubMed Link: 24036949
Variant Present in the following documents:
  • Main text
  • nihms517228.pdf
View BVdb publication page



Polymorphisms in ARMS2/HTRA1 and complement genes and age-related macular degeneration in India: findings from the INDEYE study.

Investigative Ophthalmology & Visual Science
Sundaresan, Periasamy P; Vashist, Praveen P; Ravindran, Ravilla D RD; Shanker, Ashwini A; Nitsch, Dorothea D; Nonyane, Bareng A S BA; Smeeth, Liam L; Chakravarthy, Usha U; Fletcher, Astrid E AE
Publication Date: 2012-11-01

Variant appearance in text: rs438999
PubMed Link: 23060141
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.

Human Molecular Genetics
Cipriani, Valentina V; Leung, Hin-Tak HT; Plagnol, Vincent V; Bunce, Catey C; Khan, Jane C JC; Shahid, Humma H; Moore, Anthony T AT; Harding, Simon P SP; Bishop, Paul N PN; Hayward, Caroline C; Campbell, Susan S; Armbrecht, Ana Maria AM; Dhillon, Baljean B; Deary, Ian J IJ; Campbell, Harry H; Dunlop, Malcolm M; Dominiczak, Anna F AF; Mann, Samantha S SS; Jenkins, Sharon A SA; Webster, Andrew R AR; Bird, Alan C AC; Lathrop, Mark M; Zelenika, Diana D; Souied, Eric H EH; Sahel, José-Alain JA; Léveillard, Thierry T; , ; Cree, Angela J AJ; Gibson, Jane J; Ennis, Sarah S; Lotery, Andrew J AJ; Wright, Alan F AF; Clayton, David G DG; Yates, John R W JR
Publication Date: 2012-09-15

Variant appearance in text: rs438999
PubMed Link: 22694956
Variant Present in the following documents:
  • Main text
View BVdb publication page



Modelling the genetic risk in age-related macular degeneration.

Plos One
Grassmann, Felix F; Fritsche, Lars G LG; Keilhauer, Claudia N CN; Heid, Iris M IM; Weber, Bernhard H F BH
Publication Date: 2012

Variant appearance in text: rs438999
PubMed Link: 22666427
Variant Present in the following documents:
  • Main text
  • pone.0037979.pdf
View BVdb publication page



Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.

Genes And Immunity
Kopplin, L J LJ; Igo, R P RP; Wang, Y Y; Sivakumaran, T A TA; Hagstrom, S A SA; Peachey, N S NS; Francis, P J PJ; Klein, M L ML; SanGiovanni, J P JP; Chew, E Y EY; Pauer, G J T GJ; Sturgill, G M GM; Joshi, T T; Tian, L L; Xi, Q Q; Henning, A K AK; Lee, K E KE; Klein, R R; Klein, B E K BE; Iyengar, S K SK
Publication Date: 2010-12

Variant appearance in text: rs438999
PubMed Link: 20861866
Variant Present in the following documents:
  • Main text
  • nihms206749.pdf
View BVdb publication page