rs794728360

Orientation

minus

Stabilized

minus

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

Make rs794728360(A;A)

Make rs794728360(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150958226

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728360
dbSNP (classic)	rs794728360
ClinGen	rs794728360
ebi	rs794728360
HLI	rs794728360
Exac	rs794728360
Gnomad	rs794728360
Varsome	rs794728360
LitVar	rs794728360
Map	rs794728360
PheGenI	rs794728360
Biobank	rs794728360
1000 genomes	rs794728360
hgdp	rs794728360
ensembl	rs794728360
geneview	rs794728360
scholar	rs794728360
google	rs794728360
pharmgkb	rs794728360
gwascentral	rs794728360
openSNP	rs794728360
23andMe	rs794728360
SNPshot	rs794728360
SNPdbe	rs794728360
MSV3d	rs794728360
GWAS Ctlg	rs794728360

Max Magnitude

0

ClinVar
Risk	rs794728360(A;A)
Alt	rs794728360(A;A)
Reference	Rs794728360(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150655314G>T
CLNSRC
CLNACC	RCV000181766.1,