rs794728389

Orientation

minus

Stabilized

minus

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

Make rs794728389(A;A)

Make rs794728389(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950176

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728389
dbSNP (classic)	rs794728389
ClinGen	rs794728389
ebi	rs794728389
HLI	rs794728389
Exac	rs794728389
Gnomad	rs794728389
Varsome	rs794728389
LitVar	rs794728389
Map	rs794728389
PheGenI	rs794728389
Biobank	rs794728389
1000 genomes	rs794728389
hgdp	rs794728389
ensembl	rs794728389
geneview	rs794728389
scholar	rs794728389
google	rs794728389
pharmgkb	rs794728389
gwascentral	rs794728389
openSNP	rs794728389
23andMe	rs794728389
SNPshot	rs794728389
SNPdbe	rs794728389
MSV3d	rs794728389
GWAS Ctlg	rs794728389

Max Magnitude

0

ClinVar
Risk	rs794728389(A;A)
Alt	rs794728389(A;A)
Reference	Rs794728389(C;C)
Significance	Probable-Pathogenic
Disease	not provided not specified
Variation	info
Gene	KCNH2
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000007.13:g.150647264G>T
CLNSRC
CLNACC	RCV000181856.1, RCV000223774.1,