rs794728450

Orientation

minus

Stabilized

minus

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

Make rs794728450(-;-)

Make rs794728450(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947844

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728450
dbSNP (classic)	rs794728450
ClinGen	rs794728450
ebi	rs794728450
HLI	rs794728450
Exac	rs794728450
Gnomad	rs794728450
Varsome	rs794728450
LitVar	rs794728450
Map	rs794728450
PheGenI	rs794728450
Biobank	rs794728450
1000 genomes	rs794728450
hgdp	rs794728450
ensembl	rs794728450
geneview	rs794728450
scholar	rs794728450
google	rs794728450
pharmgkb	rs794728450
gwascentral	rs794728450
openSNP	rs794728450
23andMe	rs794728450
SNPshot	rs794728450
SNPdbe	rs794728450
MSV3d	rs794728450
GWAS Ctlg	rs794728450

Max Magnitude

0

ClinVar
Risk	rs794728450(-;-)
Alt	rs794728450(-;-)
Reference	Rs794728450(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150644932delC
CLNSRC
CLNACC	RCV000181988.3,