rs199473037

Orientation

minus

Stabilized

minus

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

Make rs199473037(C;C)

Make rs199473037(C;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974780

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473037
dbSNP (classic)	rs199473037
ClinGen	rs199473037
ebi	rs199473037
HLI	rs199473037
Exac	rs199473037
Gnomad	rs199473037
Varsome	rs199473037
LitVar	rs199473037
Map	rs199473037
PheGenI	rs199473037
Biobank	rs199473037
1000 genomes	rs199473037
hgdp	rs199473037
ensembl	rs199473037
geneview	rs199473037
scholar	rs199473037
google	rs199473037
pharmgkb	rs199473037
gwascentral	rs199473037
openSNP	rs199473037
23andMe	rs199473037
SNPshot	rs199473037
SNPdbe	rs199473037
MSV3d	rs199473037
GWAS Ctlg	rs199473037

Max Magnitude

0

ClinVar
Risk	rs199473037(C;C)
Alt	rs199473037(C;C)
Reference	Rs199473037(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.150671868C>G
CLNSRC	ClinVar
CLNACC	RCV000058114.3,