rs794728453

Orientation

minus

Stabilized

minus

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

Make rs794728453(-;-)

Make rs794728453(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947807

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728453
dbSNP (classic)	rs794728453
ClinGen	rs794728453
ebi	rs794728453
HLI	rs794728453
Exac	rs794728453
Gnomad	rs794728453
Varsome	rs794728453
LitVar	rs794728453
Map	rs794728453
PheGenI	rs794728453
Biobank	rs794728453
1000 genomes	rs794728453
hgdp	rs794728453
ensembl	rs794728453
geneview	rs794728453
scholar	rs794728453
google	rs794728453
pharmgkb	rs794728453
gwascentral	rs794728453
openSNP	rs794728453
23andMe	rs794728453
SNPshot	rs794728453
SNPdbe	rs794728453
MSV3d	rs794728453
GWAS Ctlg	rs794728453

Max Magnitude

0

ClinVar
Risk	rs794728453(-;-)
Alt	rs794728453(-;-)
Reference	Rs794728453(C;C)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150644895delG
CLNSRC
CLNACC	RCV000181991.1,