rs794728407

Orientation

minus

Stabilized

minus

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

Make rs794728407(C;T)

Make rs794728407(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974899

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728407
dbSNP (classic)	rs794728407
ClinGen	rs794728407
ebi	rs794728407
HLI	rs794728407
Exac	rs794728407
Gnomad	rs794728407
Varsome	rs794728407
LitVar	rs794728407
Map	rs794728407
PheGenI	rs794728407
Biobank	rs794728407
1000 genomes	rs794728407
hgdp	rs794728407
ensembl	rs794728407
geneview	rs794728407
scholar	rs794728407
google	rs794728407
pharmgkb	rs794728407
gwascentral	rs794728407
openSNP	rs794728407
23andMe	rs794728407
SNPshot	rs794728407
SNPdbe	rs794728407
MSV3d	rs794728407
GWAS Ctlg	rs794728407

Max Magnitude

0

ClinVar
Risk	rs794728407(T;T)
Alt	rs794728407(T;T)
Reference	Rs794728407(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150671987G>A
CLNSRC
CLNACC	RCV000181924.1,