rs199473508

Orientation

minus

Stabilized

minus

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

Make rs199473508(C;C)

Make rs199473508(C;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952697

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473508
dbSNP (classic)	rs199473508
ClinGen	rs199473508
ebi	rs199473508
HLI	rs199473508
Exac	rs199473508
Gnomad	rs199473508
Varsome	rs199473508
LitVar	rs199473508
Map	rs199473508
PheGenI	rs199473508
Biobank	rs199473508
1000 genomes	rs199473508
hgdp	rs199473508
ensembl	rs199473508
geneview	rs199473508
scholar	rs199473508
google	rs199473508
pharmgkb	rs199473508
gwascentral	rs199473508
openSNP	rs199473508
23andMe	rs199473508
SNPshot	rs199473508
SNPdbe	rs199473508
MSV3d	rs199473508
GWAS Ctlg	rs199473508

Max Magnitude

0

ClinVar
Risk	rs199473508(C;C)
Alt	rs199473508(C;C)
Reference	Rs199473508(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.150649785C>G
CLNSRC	ClinVar
CLNACC	RCV000057888.3,