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LRP5 c.3764-63C>T
Variant ID: 11-68201007-C-T
NM_002335.2(
LRP5
):c.3764-63C>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:
Targeted exome sequencing identified a novel USH2A mutation in a Chinese usher syndrome family: a case report.
Bmc Ophthalmology
Xing, Dongjun D; Zhou, Huaiyu H; Yu, Rongguo R; Wang, Linni L; Hu, Liying L; Li, Zhiqing Z; Li, Xiaorong X
Publication Date: 2020-12-10
Variant appearance in text: rs12417014
PubMed Link:
33302902
Variant Present in the following documents:
12886_2020_1711_MOESM1_ESM.xlsx, sheet 1
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: rs12417014
PubMed Link:
24980784
Variant Present in the following documents:
Main text
View BVdb publication page