rs794728439

Orientation

minus

Stabilized

minus

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

Make rs794728439(-;-)

Make rs794728439(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150951717

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs794728439
dbSNP (classic)	rs794728439
ClinGen	rs794728439
ebi	rs794728439
HLI	rs794728439
Exac	rs794728439
Gnomad	rs794728439
Varsome	rs794728439
LitVar	rs794728439
Map	rs794728439
PheGenI	rs794728439
Biobank	rs794728439
1000 genomes	rs794728439
hgdp	rs794728439
ensembl	rs794728439
geneview	rs794728439
scholar	rs794728439
google	rs794728439
pharmgkb	rs794728439
gwascentral	rs794728439
openSNP	rs794728439
23andMe	rs794728439
SNPshot	rs794728439
SNPdbe	rs794728439
MSV3d	rs794728439
GWAS Ctlg	rs794728439

Max Magnitude

0

ClinVar
Risk	rs794728439(-;-)
Alt	rs794728439(-;-)
Reference	Rs794728439(T;T)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150648805delA
CLNSRC
CLNACC	RCV000181977.1,