rs199473493

Orientation

minus

Stabilized

minus

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

Make rs199473493(C;T)

Make rs199473493(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974779

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473493
dbSNP (classic)	rs199473493
ClinGen	rs199473493
ebi	rs199473493
HLI	rs199473493
Exac	rs199473493
Gnomad	rs199473493
Varsome	rs199473493
LitVar	rs199473493
Map	rs199473493
PheGenI	rs199473493
Biobank	rs199473493
1000 genomes	rs199473493
hgdp	rs199473493
ensembl	rs199473493
geneview	rs199473493
scholar	rs199473493
google	rs199473493
pharmgkb	rs199473493
gwascentral	rs199473493
openSNP	rs199473493
23andMe	rs199473493
SNPshot	rs199473493
SNPdbe	rs199473493
MSV3d	rs199473493
GWAS Ctlg	rs199473493

Max Magnitude

0

ClinVar
Risk	rs199473493(T;T)
Alt	rs199473493(T;T)
Reference	Rs199473493(C;C)
Significance	Untested
Disease	Sudden cardiac death
Variation	info
Gene	KCNH2
CLNDBN	Sudden cardiac death
Reversed	1
HGVS	NC_000007.13:g.150671867G>A
CLNSRC	ClinVar
CLNACC	RCV000058117.3,