rs794728393

Orientation

minus

Stabilized

minus

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

Make rs794728393(A;T)

Make rs794728393(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150948954

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728393
dbSNP (classic)	rs794728393
ClinGen	rs794728393
ebi	rs794728393
HLI	rs794728393
Exac	rs794728393
Gnomad	rs794728393
Varsome	rs794728393
LitVar	rs794728393
Map	rs794728393
PheGenI	rs794728393
Biobank	rs794728393
1000 genomes	rs794728393
hgdp	rs794728393
ensembl	rs794728393
geneview	rs794728393
scholar	rs794728393
google	rs794728393
pharmgkb	rs794728393
gwascentral	rs794728393
openSNP	rs794728393
23andMe	rs794728393
SNPshot	rs794728393
SNPdbe	rs794728393
MSV3d	rs794728393
GWAS Ctlg	rs794728393

Max Magnitude

0

ClinVar
Risk	rs794728393(T;T)
Alt	rs794728393(T;T)
Reference	Rs794728393(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150646042T>A
CLNSRC
CLNACC	RCV000181869.2,