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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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