rs794728488

Orientation

minus

Stabilized

minus

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

Make rs794728488(A;C)

Make rs794728488(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951122

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728488
dbSNP (classic)	rs794728488
ClinGen	rs794728488
ebi	rs794728488
HLI	rs794728488
Exac	rs794728488
Gnomad	rs794728488
Varsome	rs794728488
LitVar	rs794728488
Map	rs794728488
PheGenI	rs794728488
Biobank	rs794728488
1000 genomes	rs794728488
hgdp	rs794728488
ensembl	rs794728488
geneview	rs794728488
scholar	rs794728488
google	rs794728488
pharmgkb	rs794728488
gwascentral	rs794728488
openSNP	rs794728488
23andMe	rs794728488
SNPshot	rs794728488
SNPdbe	rs794728488
MSV3d	rs794728488
GWAS Ctlg	rs794728488

Max Magnitude

0

ClinVar
Risk	rs794728488(C;C)
Alt	rs794728488(C;C)
Reference	Rs794728488(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648210T>G
CLNSRC
CLNACC	RCV000182039.1,