rs199472797

Orientation

plus

Stabilized

plus

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

Make rs199472797(A;A)

Make rs199472797(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2775996

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472797
dbSNP (classic)	rs199472797
ClinGen	rs199472797
ebi	rs199472797
HLI	rs199472797
Exac	rs199472797
Gnomad	rs199472797
Varsome	rs199472797
LitVar	rs199472797
Map	rs199472797
PheGenI	rs199472797
Biobank	rs199472797
1000 genomes	rs199472797
hgdp	rs199472797
ensembl	rs199472797
geneview	rs199472797
scholar	rs199472797
google	rs199472797
pharmgkb	rs199472797
gwascentral	rs199472797
openSNP	rs199472797
23andMe	rs199472797
SNPshot	rs199472797
SNPdbe	rs199472797
MSV3d	rs199472797
GWAS Ctlg	rs199472797

Max Magnitude

0

ClinVar
Risk	rs199472797(A;A)
Alt	rs199472797(A;A)
Reference	Rs199472797(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2797226G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057607.3,