rs199473665

Orientation

minus

Stabilized

minus

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

Make rs199473665(C;C)

Make rs199473665(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974812

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473665
dbSNP (classic)	rs199473665
ClinGen	rs199473665
ebi	rs199473665
HLI	rs199473665
Exac	rs199473665
Gnomad	rs199473665
Varsome	rs199473665
LitVar	rs199473665
Map	rs199473665
PheGenI	rs199473665
Biobank	rs199473665
1000 genomes	rs199473665
hgdp	rs199473665
ensembl	rs199473665
geneview	rs199473665
scholar	rs199473665
google	rs199473665
pharmgkb	rs199473665
gwascentral	rs199473665
openSNP	rs199473665
23andMe	rs199473665
SNPshot	rs199473665
SNPdbe	rs199473665
MSV3d	rs199473665
GWAS Ctlg	rs199473665

Max Magnitude

0

ClinVar
Risk	rs199473665(C;C)
Alt	rs199473665(C;C)
Reference	Rs199473665(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671900A>G
CLNSRC	ClinVar
CLNACC	RCV000058078.3,