WIF1 c.398-3968A>G

Variant ID: 12-65466652-T-C

NM_007191.4(WIF1):c.398-3968A>G

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Clinical relevance of genetic polymorphisms in WNT signaling pathway (SFRP1, WNT3A, CTNNB1, WIF-1, DKK-1, LRP5, LRP6) on pulmonary tuberculosis in a Chinese population.

Frontiers In Immunology
Huang, Qian Q; Wang, Chao-Cai CC; Liu, Yun-Guang YG; Zhao, Chang-Ming CM; Zhang, Tian-Ping TP; Liu, Yan Y; Wang, Hua H
Publication Date: 2022

Variant appearance in text: rs3782499
PubMed Link: 36569862
Variant Present in the following documents:
  • Main text
  • fimmu-13-1011700.pdf
View BVdb publication page



Genetic variant of WIF1 gene is functionally associated with developmental dysplasia of the hip in Han Chinese population.

Scientific Reports
Sun, Ye Y; You, Yongqing Y; Dai, Kerong K; Zhang, Junxin J; Yan, Moqi M; Zhang, Yijian Y
Publication Date: 2019-01-22

Variant appearance in text: rs3782499
PubMed Link: 30670715
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_36532.pdf
View BVdb publication page



Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal
Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X
Publication Date: 2014-12

Variant appearance in text: rs3782499
PubMed Link: 24980784
Variant Present in the following documents:
  • Main text
View BVdb publication page