WNT3 c.81-8440A>G

Variant ID: 17-44859715-T-C

NM_030753.4(WNT3):c.81-8440A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


[Evaluating the effect of WNT pathway genes considering interactions on the risk of non-syndromic oral clefts among Chinese populations].

Beijing Da Xue Xue Bao. Yi Xue Ban = Journal Of Peking University. Health Sciences
Wang, M Y MY; Li, W Y WY; Zhou, R R; Wang, S Y SY; Liu, D J DJ; Zheng, H C HC; Li, J J; Li, N N; Zhou, Z B ZB; Zhu, H P HP; Wu, T T; Hu, Y H YH
Publication Date: 2020-10-18

Variant appearance in text: rs70602
PubMed Link: 33047713
Variant Present in the following documents:
  • Main text
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: rs70602
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics
Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT
Publication Date: 2008-07-15

Variant appearance in text: rs70602
PubMed Link: 18413325
Variant Present in the following documents:
  • Main text
View BVdb publication page