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FAM186A c.6503+5104G>A
Variant ID: 12-50739008-C-T
NM_001145475.1(
FAM186A
):c.6503+5104G>A
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:
Detection and interpretation of shared genetic influences on 42 human traits.
Nature Genetics
Pickrell, Joseph K JK; Berisa, Tomaz T; Liu, Jimmy Z JZ; Ségurel, Laure L; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2016-07
Variant appearance in text: rs4768951
PubMed Link:
27182965
Variant Present in the following documents:
NIHMS780506-supplement-11.pdf
View BVdb publication page