rs199472998

Orientation

minus

Stabilized

minus

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

Make rs199472998(G;T)

Make rs199472998(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150950168

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472998
dbSNP (classic)	rs199472998
ClinGen	rs199472998
ebi	rs199472998
HLI	rs199472998
Exac	rs199472998
Gnomad	rs199472998
Varsome	rs199472998
LitVar	rs199472998
Map	rs199472998
PheGenI	rs199472998
Biobank	rs199472998
1000 genomes	rs199472998
hgdp	rs199472998
ensembl	rs199472998
geneview	rs199472998
scholar	rs199472998
google	rs199472998
pharmgkb	rs199472998
gwascentral	rs199472998
openSNP	rs199472998
23andMe	rs199472998
SNPshot	rs199472998
SNPdbe	rs199472998
MSV3d	rs199472998
GWAS Ctlg	rs199472998

Max Magnitude

0

ClinVar
Risk	rs199472998(T;T)
Alt	rs199472998(T;T)
Reference	Rs199472998(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150647256C>A
CLNSRC	ClinVar
CLNACC	RCV000058115.3,