rs794728409

Orientation

minus

Stabilized

minus

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

Make rs794728409(G;T)

Make rs794728409(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974879

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728409
dbSNP (classic)	rs794728409
ClinGen	rs794728409
ebi	rs794728409
HLI	rs794728409
Exac	rs794728409
Gnomad	rs794728409
Varsome	rs794728409
LitVar	rs794728409
Map	rs794728409
PheGenI	rs794728409
Biobank	rs794728409
1000 genomes	rs794728409
hgdp	rs794728409
ensembl	rs794728409
geneview	rs794728409
scholar	rs794728409
google	rs794728409
pharmgkb	rs794728409
gwascentral	rs794728409
openSNP	rs794728409
23andMe	rs794728409
SNPshot	rs794728409
SNPdbe	rs794728409
MSV3d	rs794728409
GWAS Ctlg	rs794728409

Max Magnitude

0

ClinVar
Risk	rs794728409(T;T)
Alt	rs794728409(T;T)
Reference	Rs794728409(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150671967C>A
CLNSRC
CLNACC	RCV000181929.2,