rs794728477

Orientation

minus

Stabilized

minus

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

Make rs794728477(C;C)

Make rs794728477(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150959571

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728477
dbSNP (classic)	rs794728477
ClinGen	rs794728477
ebi	rs794728477
HLI	rs794728477
Exac	rs794728477
Gnomad	rs794728477
Varsome	rs794728477
LitVar	rs794728477
Map	rs794728477
PheGenI	rs794728477
Biobank	rs794728477
1000 genomes	rs794728477
hgdp	rs794728477
ensembl	rs794728477
geneview	rs794728477
scholar	rs794728477
google	rs794728477
pharmgkb	rs794728477
gwascentral	rs794728477
openSNP	rs794728477
23andMe	rs794728477
SNPshot	rs794728477
SNPdbe	rs794728477
MSV3d	rs794728477
GWAS Ctlg	rs794728477

Max Magnitude

0

ClinVar
Risk	rs794728477(A;A) rs794728477(C;C)
Alt	rs794728477(A;A) rs794728477(C;C)
Reference	Rs794728477(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150656659C>T
CLNSRC
CLNACC	RCV000483249.1,