rs199472874

Orientation

minus

Stabilized

minus

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

Make rs199472874(A;A)

Make rs199472874(A;C)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150958221

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472874
dbSNP (classic)	rs199472874
ClinGen	rs199472874
ebi	rs199472874
HLI	rs199472874
Exac	rs199472874
Gnomad	rs199472874
Varsome	rs199472874
LitVar	rs199472874
Map	rs199472874
PheGenI	rs199472874
Biobank	rs199472874
1000 genomes	rs199472874
hgdp	rs199472874
ensembl	rs199472874
geneview	rs199472874
scholar	rs199472874
google	rs199472874
pharmgkb	rs199472874
gwascentral	rs199472874
openSNP	rs199472874
23andMe	rs199472874
SNPshot	rs199472874
SNPdbe	rs199472874
MSV3d	rs199472874
GWAS Ctlg	rs199472874

Max Magnitude

0

ClinVar
Risk	rs199472874(A;A) rs199472874(G;G) rs199472874(T;T)
Alt	rs199472874(A;A) rs199472874(G;G) rs199472874(T;T)
Reference	Rs199472874(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150655309G>C
CLNSRC	ClinVar
CLNACC	RCV000058253.3,