Bibliome.ai browser hg19
Search
About
Stats
FAQ
AKAP13 c.-11-27835C>G
Variant ID: 15-86001106-C-G
NM_007200.4(
AKAP13
):c.-11-27835C>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:
Genomics and genome-wide association studies: an integrative approach to expression QTL mapping.
Genomics
Degnan, James H JH; Lasky-Su, Jessica J; Raby, Benjamin A BA; Xu, Mousheng M; Molony, Cliona C; Schadt, Eric E EE; Lange, Christoph C
Publication Date: 2008-09
Variant appearance in text: rs1968867
PubMed Link:
18586451
Variant Present in the following documents:
Main text
View BVdb publication page