WNT3 c.81-7869G>A

Variant ID: 17-44859144-C-T

NM_030753.4(WNT3):c.81-7869G>A

This variant was identified in 13 publications

View GRCh38 version.




Publications:


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: rs415430
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.

Communications Biology
Sarnowski, Chloé C; Ghanbari, Mohsen M; Bis, Joshua C JC; Logue, Mark M; Fornage, Myriam M; Mishra, Aniket A; Ahmad, Shahzad S; Beiser, Alexa S AS; Boerwinkle, Eric E; Bouteloup, Vincent V; Chouraki, Vincent V; Cupples, L Adrienne LA; Damotte, Vincent V; DeCarli, Charles S CS; DeStefano, Anita L AL; Djoussé, Luc L; Fohner, Alison E AE; Franz, Carol E CE; Kautz, Tiffany F TF; Lambert, Jean-Charles JC; Lyons, Michael J MJ; Mosley, Thomas H TH; Mukamal, Kenneth J KJ; Pase, Matthew P MP; Portilla Fernandez, Eliana C EC; Rissman, Robert A RA; Satizabal, Claudia L CL; Vasan, Ramachandran S RS; Yaqub, Amber A; Debette, Stephanie S; Dufouil, Carole C; Launer, Lenore J LJ; Kremen, William S WS; Longstreth, William T WT; Ikram, M Arfan MA; Seshadri, Sudha S
Publication Date: 2022-04-08

Variant appearance in text: rs415430
PubMed Link: 35396452
Variant Present in the following documents:
  • 42003_2022_3287_MOESM1_ESM.pdf
View BVdb publication page



Association Analysis of WNT3, HLA-DRB5 and IL1R2 Polymorphisms in Chinese Patients With Parkinson's Disease and Multiple System Atrophy.

Frontiers In Genetics
Su, Wei-Ming WM; Gu, Xiao-Jing XJ; Hou, Yan-Bing YB; Zhang, Ling-Yu LY; Cao, Bei B; Ou, Ru-Wei RW; Wu, Ying Y; Chen, Xue-Ping XP; Song, Wei W; Zhao, Bi B; Shang, Hui-Fang HF; Chen, Yong-Ping YP
Publication Date: 2021

Variant appearance in text: rs415430
PubMed Link: 34868249
Variant Present in the following documents:
  • Main text
View BVdb publication page



Heritability Enrichment of Immunoglobulin G N-Glycosylation in Specific Tissues.

Frontiers In Immunology
Li, Xingang X; Wang, Hao H; Zhu, Yahong Y; Cao, Weijie W; Song, Manshu M; Wang, Youxin Y; Hou, Haifeng H; Lang, Minglin M; Guo, Xiuhua X; Tan, Xuerui X; Han, Jingdong J JJ; Wang, Wei W
Publication Date: 2021

Variant appearance in text: rs415430
PubMed Link: 34804021
Variant Present in the following documents:
  • Main text
  • fimmu-12-741705.pdf
View BVdb publication page



Shared Genetic Background between Parkinson's Disease and Schizophrenia: A Two-Sample Mendelian Randomization Study.

Brain Sciences
Kim, Kiwon K; Kim, Soyeon S; Myung, Woojae W; Shim, Injeong I; Lee, Hyewon H; Kim, Beomsu B; Cho, Sung Kweon SK; Yoon, Joohyun J; Kim, Doh Kwan DK; Won, Hong-Hee HH
Publication Date: 2021-08-06

Variant appearance in text: rs415430
PubMed Link: 34439661
Variant Present in the following documents:
  • Main text
  • brainsci-11-01042.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs415430
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

Frontiers In Genetics
Wallace, Amelia D AD; Wendt, George A GA; Barcellos, Lisa F LF; de Smith, Adam J AJ; Walsh, Kyle M KM; Metayer, Catherine C; Costello, Joseph F JF; Wiemels, Joseph L JL; Francis, Stephen S SS
Publication Date: 2018

Variant appearance in text: rs415430
PubMed Link: 30154825
Variant Present in the following documents:
  • Main text
  • fgene-09-00298.pdf
View BVdb publication page



GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.

Molecular Psychiatry
Trampush, J W JW; Yang, M L Z ML; Yu, J J; Knowles, E E; Davies, G G; Liewald, D C DC; Starr, J M JM; Djurovic, S S; Melle, I I; Sundet, K K; Christoforou, A A; Reinvang, I I; DeRosse, P P; Lundervold, A J AJ; Steen, V M VM; Espeseth, T T; Räikkönen, K K; Widen, E E; Palotie, A A; Eriksson, J G JG; Giegling, I I; Konte, B B; Roussos, P P; Giakoumaki, S S; Burdick, K E KE; Payton, A A; Ollier, W W; Horan, M M; Chiba-Falek, O O; Attix, D K DK; Need, A C AC; Cirulli, E T ET; Voineskos, A N AN; Stefanis, N C NC; Avramopoulos, D D; Hatzimanolis, A A; Arking, D E DE; Smyrnis, N N; Bilder, R M RM; Freimer, N A NA; Cannon, T D TD; London, E E; Poldrack, R A RA; Sabb, F W FW; Congdon, E E; Conley, E D ED; Scult, M A MA; Dickinson, D D; Straub, R E RE; Donohoe, G G; Morris, D D; Corvin, A A; Gill, M M; Hariri, A R AR; Weinberger, D R DR; Pendleton, N N; Bitsios, P P; Rujescu, D D; Lahti, J J; Le Hellard, S S; Keller, M C MC; Andreassen, O A OA; Deary, I J IJ; Glahn, D C DC; Malhotra, A K AK; Lencz, T T
Publication Date: 2017-03

Variant appearance in text: rs415430
PubMed Link: 28093568
Variant Present in the following documents:
  • mp2016244x2.xlsx, sheet 2
View BVdb publication page



Alternate-locus aware variant calling in whole genome sequencing.

Genome Medicine
Jäger, Marten M; Schubach, Max M; Zemojtel, Tomasz T; Reinert, Knut K; Church, Deanna M DM; Robinson, Peter N PN
Publication Date: 2016-12-13

Variant appearance in text: rs415430
PubMed Link: 27964746
Variant Present in the following documents:
  • 13073_2016_383_MOESM1_ESM.pdf
View BVdb publication page



Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank.

The Lancet. Respiratory Medicine
Wain, Louise V LV; Shrine, Nick N; Miller, Suzanne S; Jackson, Victoria E VE; Ntalla, Ioanna I; Soler Artigas, María M; Billington, Charlotte K CK; Kheirallah, Abdul Kader AK; Allen, Richard R; Cook, James P JP; Probert, Kelly K; Obeidat, Ma'en M; Bossé, Yohan Y; Hao, Ke K; Postma, Dirkje S DS; Paré, Peter D PD; Ramasamy, Adaikalavan A; , ; Mägi, Reedik R; Mihailov, Evelin E; Reinmaa, Eva E; Melén, Erik E; O'Connell, Jared J; Frangou, Eleni E; Delaneau, Olivier O; , ; Freeman, Colin C; Petkova, Desislava D; McCarthy, Mark M; Sayers, Ian I; Deloukas, Panos P; Hubbard, Richard R; Pavord, Ian I; Hansell, Anna L AL; Thomson, Neil C NC; Zeggini, Eleftheria E; Morris, Andrew P AP; Marchini, Jonathan J; Strachan, David P DP; Tobin, Martin D MD; Hall, Ian P IP
Publication Date: 2015-10

Variant appearance in text: rs415430
PubMed Link: 26423011
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page



Human disease-associated genetic variation impacts large intergenic non-coding RNA expression.

Plos Genetics
Kumar, Vinod V; Westra, Harm-Jan HJ; Karjalainen, Juha J; Zhernakova, Daria V DV; Esko, Tõnu T; Hrdlickova, Barbara B; Almeida, Rodrigo R; Zhernakova, Alexandra A; Reinmaa, Eva E; Võsa, Urmo U; Hofker, Marten H MH; Fehrmann, Rudolf S N RS; Fu, Jingyuan J; Withoff, Sebo S; Metspalu, Andres A; Franke, Lude L; Wijmenga, Cisca C
Publication Date: 2013

Variant appearance in text: rs415430
PubMed Link: 23341781
Variant Present in the following documents:
  • Main text
  • pgen.1003201.pdf
View BVdb publication page



Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.

Bmc Medical Genetics
Liu, Xinmin X; Cheng, Rong R; Verbitsky, Miguel M; Kisselev, Sergey S; Browne, Andrew A; Mejia-Sanatana, Helen H; Louis, Elan D ED; Cote, Lucien J LJ; Andrews, Howard H; Waters, Cheryl C; Ford, Blair B; Frucht, Steven S; Fahn, Stanley S; Marder, Karen K; Clark, Lorraine N LN; Lee, Joseph H JH
Publication Date: 2011-08-03

Variant appearance in text: rs415430
PubMed Link: 21812969
Variant Present in the following documents:
  • Main text
  • 1471-2350-12-104.pdf
View BVdb publication page



Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

Nature Genetics
Hamza, Taye H TH; Zabetian, Cyrus P CP; Tenesa, Albert A; Laederach, Alain A; Montimurro, Jennifer J; Yearout, Dora D; Kay, Denise M DM; Doheny, Kimberly F KF; Paschall, Justin J; Pugh, Elizabeth E; Kusel, Victoria I VI; Collura, Randall R; Roberts, John J; Griffith, Alida A; Samii, Ali A; Scott, William K WK; Nutt, John J; Factor, Stewart A SA; Payami, Haydeh H
Publication Date: 2010-09

Variant appearance in text: rs415430
PubMed Link: 20711177
Variant Present in the following documents:
  • NIHMS222438-supplement-1.pdf
View BVdb publication page