rs199473013

Orientation

minus

Stabilized

minus

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

Make rs199473013(A;A)

Make rs199473013(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947692

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473013
dbSNP (classic)	rs199473013
ClinGen	rs199473013
ebi	rs199473013
HLI	rs199473013
Exac	rs199473013
Gnomad	rs199473013
Varsome	rs199473013
LitVar	rs199473013
Map	rs199473013
PheGenI	rs199473013
Biobank	rs199473013
1000 genomes	rs199473013
hgdp	rs199473013
ensembl	rs199473013
geneview	rs199473013
scholar	rs199473013
google	rs199473013
pharmgkb	rs199473013
gwascentral	rs199473013
openSNP	rs199473013
23andMe	rs199473013
SNPshot	rs199473013
SNPdbe	rs199473013
MSV3d	rs199473013
GWAS Ctlg	rs199473013

Max Magnitude

0

ClinVar
Risk	rs199473013(A;A)
Alt	rs199473013(A;A)
Reference	Rs199473013(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.150644780C>T
CLNSRC	ClinVar
CLNACC	RCV000058174.3,