rs199472959

Orientation

minus

Stabilized

minus

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

Make rs199472959(G;G)

Make rs199472959(G;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951502

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472959
dbSNP (classic)	rs199472959
ClinGen	rs199472959
ebi	rs199472959
HLI	rs199472959
Exac	rs199472959
Gnomad	rs199472959
Varsome	rs199472959
LitVar	rs199472959
Map	rs199472959
PheGenI	rs199472959
Biobank	rs199472959
1000 genomes	rs199472959
hgdp	rs199472959
ensembl	rs199472959
geneview	rs199472959
scholar	rs199472959
google	rs199472959
pharmgkb	rs199472959
gwascentral	rs199472959
openSNP	rs199472959
23andMe	rs199472959
SNPshot	rs199472959
SNPdbe	rs199472959
MSV3d	rs199472959
GWAS Ctlg	rs199472959

Max Magnitude

0

ClinVar
Risk	rs199472959(G;G)
Alt	rs199472959(G;G)
Reference	Rs199472959(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648590A>C
CLNSRC	ClinVar
CLNACC	RCV000058039.3,