rs794728382

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	5	Romano-Ward Long QT Syndrome

Make rs794728382(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950962

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728382
dbSNP (classic)	rs794728382
ClinGen	rs794728382
ebi	rs794728382
HLI	rs794728382
Exac	rs794728382
Gnomad	rs794728382
Varsome	rs794728382
LitVar	rs794728382
Map	rs794728382
PheGenI	rs794728382
Biobank	rs794728382
1000 genomes	rs794728382
hgdp	rs794728382
ensembl	rs794728382
geneview	rs794728382
scholar	rs794728382
google	rs794728382
pharmgkb	rs794728382
gwascentral	rs794728382
openSNP	rs794728382
23andMe	rs794728382
SNPshot	rs794728382
SNPdbe	rs794728382
MSV3d	rs794728382
GWAS Ctlg	rs794728382

Max Magnitude

5

ClinVar
Risk	rs794728382(T;T)
Alt	rs794728382(T;T)
Reference	Rs794728382(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648050G>A
CLNSRC
CLNACC	RCV000181835.1,