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ABCG8 c.1756+685T>C
Variant ID: 2-44103237-T-C
NM_022437.2(
ABCG8
):c.1756+685T>C
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:
Generalized multifactor dimensionality reduction approaches to identification of genetic interactions underlying ordinal traits.
Genetic Epidemiology
Hou, Ting-Ting TT; Lin, Feng F; Bai, Shasha S; Cleves, Mario A MA; Xu, Hai-Ming HM; Lou, Xiang-Yang XY
Publication Date: 2019-02
Variant appearance in text: rs17606027
PubMed Link:
30387901
Variant Present in the following documents:
Main text
View BVdb publication page