rs199472736

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs199472736(A;A)

Make rs199472736(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2572940

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472736
dbSNP (classic)	rs199472736
ClinGen	rs199472736
ebi	rs199472736
HLI	rs199472736
Exac	rs199472736
Gnomad	rs199472736
Varsome	rs199472736
LitVar	rs199472736
Map	rs199472736
PheGenI	rs199472736
Biobank	rs199472736
1000 genomes	rs199472736
hgdp	rs199472736
ensembl	rs199472736
geneview	rs199472736
scholar	rs199472736
google	rs199472736
pharmgkb	rs199472736
gwascentral	rs199472736
openSNP	rs199472736
23andMe	rs199472736
SNPshot	rs199472736
SNPdbe	rs199472736
MSV3d	rs199472736
GWAS Ctlg	rs199472736

Max Magnitude

0

ClinVar
Risk	rs199472736(A;A)
Alt	rs199472736(A;A)
Reference	Rs199472736(G;G)
Significance	Untested
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome not specified
Reversed	0
HGVS	NC_000011.9:g.2594170G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057784.3, RCV000182126.3,