Bibliome.ai browser hg19
Search
About
Stats
FAQ
WNT9B c.78-5055G>T
Variant ID: 17-44944828-G-T
NM_003396.1(
WNT9B
):c.78-5055G>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
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: rs6504591
PubMed Link:
24980784
Variant Present in the following documents:
Main text
View BVdb publication page