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APOB c.2816+1086C>T
Variant ID: 2-21244617-G-A
NM_000384.2(
APOB
):c.2816+1086C>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:
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: rs12720791
PubMed Link:
19336475
Variant Present in the following documents:
ddp159_1.pdf
View BVdb publication page