rs794728499

Orientation

minus

Stabilized

minus

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

Make rs794728499(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951578

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728499
dbSNP (classic)	rs794728499
ClinGen	rs794728499
ebi	rs794728499
HLI	rs794728499
Exac	rs794728499
Gnomad	rs794728499
Varsome	rs794728499
LitVar	rs794728499
Map	rs794728499
PheGenI	rs794728499
Biobank	rs794728499
1000 genomes	rs794728499
hgdp	rs794728499
ensembl	rs794728499
geneview	rs794728499
scholar	rs794728499
google	rs794728499
pharmgkb	rs794728499
gwascentral	rs794728499
openSNP	rs794728499
23andMe	rs794728499
SNPshot	rs794728499
SNPdbe	rs794728499
MSV3d	rs794728499
GWAS Ctlg	rs794728499

Max Magnitude

5

ClinVar
Risk	rs794728499(-;-)
Alt	rs794728499(-;-)
Reference	Rs794728499(C;C)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150648666delG
CLNSRC
CLNACC	RCV000182058.1,