Bibliome.ai browser hg19
Search
About
Stats
FAQ
KCNH2 c.1128+1691G>A
Variant ID: 7-150652688-C-T
NM_000238.3(
KCNH2
):c.1128+1691G>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:
In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).
Genomic Medicine
Sudandiradoss, C C; Sethumadhavan, Rao R
Publication Date: 2008-12
Variant appearance in text: rs41311012
PubMed Link:
19214780
Variant Present in the following documents:
Main text
View BVdb publication page