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ABCB11 c.3412-1083T>G
Variant ID: 2-169784955-A-C
NM_003742.2(
ABCB11
):c.3412-1083T>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:
Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits.
Computational And Mathematical Methods In Medicine
Wu, Baolin B; Pankow, James S JS
Publication Date: 2018
Variant appearance in text: rs508506
PubMed Link:
29743933
Variant Present in the following documents:
2564531.f1.pdf
View BVdb publication page