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KCNQ1 c.-40G>A
Variant ID: 11-2466289-G-A
NM_000218.2(
KCNQ1
):c.-40G>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: rs45504094
PubMed Link:
19214780
Variant Present in the following documents:
Main text
View BVdb publication page