WNT3 c.81-8746G>C

Variant ID: 17-44860021-C-G

NM_030753.4(WNT3):c.81-8746G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs70600
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.

Nature Genetics
Hysi, Pirro G PG; Choquet, Hélène H; Khawaja, Anthony P AP; Wojciechowski, Robert R; Tedja, Milly S MS; Yin, Jie J; Simcoe, Mark J MJ; Patasova, Karina K; Mahroo, Omar A OA; Thai, Khanh K KK; Cumberland, Phillippa M PM; Melles, Ronald B RB; Verhoeven, Virginie J M VJM; Vitart, Veronique V; Segre, Ayellet A; Stone, Richard A RA; Wareham, Nick N; Hewitt, Alex W AW; Mackey, David A DA; Klaver, Caroline C W CCW; MacGregor, Stuart S; , ; Khaw, Peng T PT; Foster, Paul J PJ; , ; Guggenheim, Jeremy A JA; , ; Rahi, Jugnoo S JS; Jorgenson, Eric E; Hammond, Christopher J CJ
Publication Date: 2020-04

Variant appearance in text: rs70600
PubMed Link: 32231278
Variant Present in the following documents:
  • Main text
  • EMS85881.pdf
View BVdb publication page