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ABCG8 c.1795_1796delinsAC ;(p.C599T)
Variant ID: 2-44104738-TG-AC
NM_022437.2(
ABCG8
):c.1795_1796delinsAC;(p.C599T)
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:
Genetics of coronary artery disease and myocardial infarction.
World Journal Of Cardiology
Dai, Xuming X; Wiernek, Szymon S; Evans, James P JP; Runge, Marschall S MS
Publication Date: 2016-01-26
Variant appearance in text: ABCG8: C599T
PubMed Link:
26839654
Variant Present in the following documents:
Main text
View BVdb publication page