rs794728496

Orientation

minus

Stabilized

minus

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

Make rs794728496(-;-)

Make rs794728496(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150958297

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728496
dbSNP (classic)	rs794728496
ClinGen	rs794728496
ebi	rs794728496
HLI	rs794728496
Exac	rs794728496
Gnomad	rs794728496
Varsome	rs794728496
LitVar	rs794728496
Map	rs794728496
PheGenI	rs794728496
Biobank	rs794728496
1000 genomes	rs794728496
hgdp	rs794728496
ensembl	rs794728496
geneview	rs794728496
scholar	rs794728496
google	rs794728496
pharmgkb	rs794728496
gwascentral	rs794728496
openSNP	rs794728496
23andMe	rs794728496
SNPshot	rs794728496
SNPdbe	rs794728496
MSV3d	rs794728496
GWAS Ctlg	rs794728496

Max Magnitude

0

ClinVar
Risk	rs794728496(-;-)
Alt	rs794728496(-;-)
Reference	Rs794728496(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150655385delC
CLNSRC
CLNACC	RCV000182055.1,