rs199472932

Orientation

minus

Stabilized

minus

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

Make rs199472932(A;G)

Make rs199472932(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951610

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472932
dbSNP (classic)	rs199472932
ClinGen	rs199472932
ebi	rs199472932
HLI	rs199472932
Exac	rs199472932
Gnomad	rs199472932
Varsome	rs199472932
LitVar	rs199472932
Map	rs199472932
PheGenI	rs199472932
Biobank	rs199472932
1000 genomes	rs199472932
hgdp	rs199472932
ensembl	rs199472932
geneview	rs199472932
scholar	rs199472932
google	rs199472932
pharmgkb	rs199472932
gwascentral	rs199472932
openSNP	rs199472932
23andMe	rs199472932
SNPshot	rs199472932
SNPdbe	rs199472932
MSV3d	rs199472932
GWAS Ctlg	rs199472932

Max Magnitude

0

ClinVar
Risk	rs199472932(G;G)
Alt	rs199472932(G;G)
Reference	Rs199472932(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648698T>C
CLNSRC	ClinVar
CLNACC	RCV000057988.3,