rs794728436

Orientation

minus

Stabilized

minus

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

Make rs794728436(-;C)

Make rs794728436(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952662

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728436
dbSNP (classic)	rs794728436
ClinGen	rs794728436
ebi	rs794728436
HLI	rs794728436
Exac	rs794728436
Gnomad	rs794728436
Varsome	rs794728436
LitVar	rs794728436
Map	rs794728436
PheGenI	rs794728436
Biobank	rs794728436
1000 genomes	rs794728436
hgdp	rs794728436
ensembl	rs794728436
geneview	rs794728436
scholar	rs794728436
google	rs794728436
pharmgkb	rs794728436
gwascentral	rs794728436
openSNP	rs794728436
23andMe	rs794728436
SNPshot	rs794728436
SNPdbe	rs794728436
MSV3d	rs794728436
GWAS Ctlg	rs794728436

Max Magnitude

0

ClinVar
Risk	rs794728436(C;C)
Alt	rs794728436(C;C)
Reference	Rs794728436(-;-)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150649751dupG
CLNSRC
CLNACC	RCV000181974.1,