rs199473514

Orientation

minus

Stabilized

minus

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

Make rs199473514(A;A)

Make rs199473514(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951829

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473514
dbSNP (classic)	rs199473514
ClinGen	rs199473514
ebi	rs199473514
HLI	rs199473514
Exac	rs199473514
Gnomad	rs199473514
Varsome	rs199473514
LitVar	rs199473514
Map	rs199473514
PheGenI	rs199473514
Biobank	rs199473514
1000 genomes	rs199473514
hgdp	rs199473514
ensembl	rs199473514
geneview	rs199473514
scholar	rs199473514
google	rs199473514
pharmgkb	rs199473514
gwascentral	rs199473514
openSNP	rs199473514
23andMe	rs199473514
SNPshot	rs199473514
SNPdbe	rs199473514
MSV3d	rs199473514
GWAS Ctlg	rs199473514

Max Magnitude

0

ClinVar
Risk	rs199473514(A;A)
Alt	rs199473514(A;A)
Reference	Rs199473514(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.150648917C>T
CLNSRC	ClinVar
CLNACC	RCV000057921.3,