rs199473667

Orientation

minus

Stabilized

minus

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

Make rs199473667(A;G)

Make rs199473667(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951673

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473667
dbSNP (classic)	rs199473667
ClinGen	rs199473667
ebi	rs199473667
HLI	rs199473667
Exac	rs199473667
Gnomad	rs199473667
Varsome	rs199473667
LitVar	rs199473667
Map	rs199473667
PheGenI	rs199473667
Biobank	rs199473667
1000 genomes	rs199473667
hgdp	rs199473667
ensembl	rs199473667
geneview	rs199473667
scholar	rs199473667
google	rs199473667
pharmgkb	rs199473667
gwascentral	rs199473667
openSNP	rs199473667
23andMe	rs199473667
SNPshot	rs199473667
SNPdbe	rs199473667
MSV3d	rs199473667
GWAS Ctlg	rs199473667

Max Magnitude

0

ClinVar
Risk	rs199473667(C;C) rs199473667(G;G)
Alt	rs199473667(C;C) rs199473667(G;G)
Reference	Rs199473667(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648761T>C
CLNSRC	ClinVar
CLNACC	RCV000057964.3,