rs794728483

Orientation

minus

Stabilized

minus

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

Make rs794728483(A;A)

Make rs794728483(A;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951651

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728483
dbSNP (classic)	rs794728483
ClinGen	rs794728483
ebi	rs794728483
HLI	rs794728483
Exac	rs794728483
Gnomad	rs794728483
Varsome	rs794728483
LitVar	rs794728483
Map	rs794728483
PheGenI	rs794728483
Biobank	rs794728483
1000 genomes	rs794728483
hgdp	rs794728483
ensembl	rs794728483
geneview	rs794728483
scholar	rs794728483
google	rs794728483
pharmgkb	rs794728483
gwascentral	rs794728483
openSNP	rs794728483
23andMe	rs794728483
SNPshot	rs794728483
SNPdbe	rs794728483
MSV3d	rs794728483
GWAS Ctlg	rs794728483

Max Magnitude

0

ClinVar
Risk	rs794728483(A;A)
Alt	rs794728483(A;A)
Reference	Rs794728483(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648739G>T
CLNSRC
CLNACC	RCV000182028.1,