WNT3 c.323-293G>C

Variant ID: 17-44847707-C-G

NM_030753.4(WNT3):c.323-293G>C

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Shared genetic links between frontotemporal dementia and psychiatric disorders.

Bmc Medicine
Li, Chunyu C; Pang, Dejiang D; Lin, Junyu J; Yang, Tianmi T; Shang, Huifang H
Publication Date: 2022-05-05

Variant appearance in text: rs199526
PubMed Link: 35509074
Variant Present in the following documents:
  • Main text
  • 12916_2022_Article_2335.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: rs199526
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



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: WNT3: 323-293G>C; rs199526
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.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: rs199526
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
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: rs199526
PubMed Link: 26423011
Variant Present in the following documents:
  • mmc1.pdf
View BVdb publication page