rs794728364

Orientation

minus

Stabilized

minus

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

Make rs794728364(C;T)

Make rs794728364(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150957323

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728364
dbSNP (classic)	rs794728364
ClinGen	rs794728364
ebi	rs794728364
HLI	rs794728364
Exac	rs794728364
Gnomad	rs794728364
Varsome	rs794728364
LitVar	rs794728364
Map	rs794728364
PheGenI	rs794728364
Biobank	rs794728364
1000 genomes	rs794728364
hgdp	rs794728364
ensembl	rs794728364
geneview	rs794728364
scholar	rs794728364
google	rs794728364
pharmgkb	rs794728364
gwascentral	rs794728364
openSNP	rs794728364
23andMe	rs794728364
SNPshot	rs794728364
SNPdbe	rs794728364
MSV3d	rs794728364
GWAS Ctlg	rs794728364

Max Magnitude

0

ClinVar
Risk	rs794728364(T;T)
Alt	rs794728364(T;T)
Reference	Rs794728364(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150654411G>A
CLNSRC
CLNACC	RCV000181779.2,