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PCSK7 c.1054+381A>G
Variant ID: 11-117094413-T-C
NM_004716.2(
PCSK7
):c.1054+381A>G
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:
Multiple phenotype association tests using summary statistics in genome-wide association studies.
Biometrics
Liu, Zhonghua Z; Lin, Xihong X
Publication Date: 2018-03
Variant appearance in text: rs11216321
PubMed Link:
28653391
Variant Present in the following documents:
Main text
View BVdb publication page