rs794728388

Orientation

minus

Stabilized

minus

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

Make rs794728388(C;C)

Make rs794728388(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150950200

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728388
dbSNP (classic)	rs794728388
ClinGen	rs794728388
ebi	rs794728388
HLI	rs794728388
Exac	rs794728388
Gnomad	rs794728388
Varsome	rs794728388
LitVar	rs794728388
Map	rs794728388
PheGenI	rs794728388
Biobank	rs794728388
1000 genomes	rs794728388
hgdp	rs794728388
ensembl	rs794728388
geneview	rs794728388
scholar	rs794728388
google	rs794728388
pharmgkb	rs794728388
gwascentral	rs794728388
openSNP	rs794728388
23andMe	rs794728388
SNPshot	rs794728388
SNPdbe	rs794728388
MSV3d	rs794728388
GWAS Ctlg	rs794728388

Max Magnitude

0

ClinVar
Risk	rs794728388(C;C)
Alt	rs794728388(C;C)
Reference	Rs794728388(T;T)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150647288A>G
CLNSRC
CLNACC	RCV000181851.1,