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LRP5 c.92-13315A>T
Variant ID: 11-68102000-A-T
NM_002335.2(
LRP5
):c.92-13315A>T
This variant was identified in 2 publications
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: rs606989
PubMed Link:
24980784
Variant Present in the following documents:
Main text
View BVdb publication page
Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.
Human Molecular Genetics
Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD
Publication Date: 2009-06-15
Variant appearance in text: rs606989
PubMed Link:
19336475
Variant Present in the following documents:
ddp159_1.pdf
View BVdb publication page