rs794728372

Orientation

minus

Stabilized

minus

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

Make rs794728372(C;T)

Make rs794728372(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150952462

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728372
dbSNP (classic)	rs794728372
ClinGen	rs794728372
ebi	rs794728372
HLI	rs794728372
Exac	rs794728372
Gnomad	rs794728372
Varsome	rs794728372
LitVar	rs794728372
Map	rs794728372
PheGenI	rs794728372
Biobank	rs794728372
1000 genomes	rs794728372
hgdp	rs794728372
ensembl	rs794728372
geneview	rs794728372
scholar	rs794728372
google	rs794728372
pharmgkb	rs794728372
gwascentral	rs794728372
openSNP	rs794728372
23andMe	rs794728372
SNPshot	rs794728372
SNPdbe	rs794728372
MSV3d	rs794728372
GWAS Ctlg	rs794728372

Max Magnitude

0

ClinVar
Risk	rs794728372(T;T)
Alt	rs794728372(T;T)
Reference	Rs794728372(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	KCNH2
CLNDBN	not specified
Reversed	1
HGVS	NC_000007.13:g.150649550G>A
CLNSRC
CLNACC	RCV000181797.3,