rs794728435

Orientation

minus

Stabilized

minus

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

Make rs794728435(-;-)

Make rs794728435(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952666

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728435
dbSNP (classic)	rs794728435
ClinGen	rs794728435
ebi	rs794728435
HLI	rs794728435
Exac	rs794728435
Gnomad	rs794728435
Varsome	rs794728435
LitVar	rs794728435
Map	rs794728435
PheGenI	rs794728435
Biobank	rs794728435
1000 genomes	rs794728435
hgdp	rs794728435
ensembl	rs794728435
geneview	rs794728435
scholar	rs794728435
google	rs794728435
pharmgkb	rs794728435
gwascentral	rs794728435
openSNP	rs794728435
23andMe	rs794728435
SNPshot	rs794728435
SNPdbe	rs794728435
MSV3d	rs794728435
GWAS Ctlg	rs794728435

Max Magnitude

0

ClinVar
Risk	rs794728435(-;-)
Alt	rs794728435(-;-)
Reference	Rs794728435(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150649754delC
CLNSRC
CLNACC	RCV000181973.2,