rs794728378

Orientation

minus

Stabilized

minus

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

Make rs794728378(A;G)

Make rs794728378(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951480

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728378
dbSNP (classic)	rs794728378
ClinGen	rs794728378
ebi	rs794728378
HLI	rs794728378
Exac	rs794728378
Gnomad	rs794728378
Varsome	rs794728378
LitVar	rs794728378
Map	rs794728378
PheGenI	rs794728378
Biobank	rs794728378
1000 genomes	rs794728378
hgdp	rs794728378
ensembl	rs794728378
geneview	rs794728378
scholar	rs794728378
google	rs794728378
pharmgkb	rs794728378
gwascentral	rs794728378
openSNP	rs794728378
23andMe	rs794728378
SNPshot	rs794728378
SNPdbe	rs794728378
MSV3d	rs794728378
GWAS Ctlg	rs794728378

Max Magnitude

0

ClinVar
Risk	rs794728378(G;G)
Alt	rs794728378(G;G)
Reference	Rs794728378(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNH2
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.150648568T>C
CLNSRC
CLNACC	RCV000181828.1,