rs794728431

Orientation

minus

Stabilized

minus

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

Make rs794728431(-;-)

Make rs794728431(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150957405

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728431
dbSNP (classic)	rs794728431
ClinGen	rs794728431
ebi	rs794728431
HLI	rs794728431
Exac	rs794728431
Gnomad	rs794728431
Varsome	rs794728431
LitVar	rs794728431
Map	rs794728431
PheGenI	rs794728431
Biobank	rs794728431
1000 genomes	rs794728431
hgdp	rs794728431
ensembl	rs794728431
geneview	rs794728431
scholar	rs794728431
google	rs794728431
pharmgkb	rs794728431
gwascentral	rs794728431
openSNP	rs794728431
23andMe	rs794728431
SNPshot	rs794728431
SNPdbe	rs794728431
MSV3d	rs794728431
GWAS Ctlg	rs794728431

Max Magnitude

0

ClinVar
Risk	rs794728431(-;-)
Alt	rs794728431(-;-)
Reference	Rs794728431(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150654493delG
CLNSRC
CLNACC	RCV000181969.1,