rs794728508

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;T)	5	Romano-Ward Long QT Syndrome
(T;T)	0	common in clinvar

Make rs794728508(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150974864

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs794728508
dbSNP (classic)	rs794728508
ClinGen	rs794728508
ebi	rs794728508
HLI	rs794728508
Exac	rs794728508
Gnomad	rs794728508
Varsome	rs794728508
LitVar	rs794728508
Map	rs794728508
PheGenI	rs794728508
Biobank	rs794728508
1000 genomes	rs794728508
hgdp	rs794728508
ensembl	rs794728508
geneview	rs794728508
scholar	rs794728508
google	rs794728508
pharmgkb	rs794728508
gwascentral	rs794728508
openSNP	rs794728508
23andMe	rs794728508
SNPshot	rs794728508
SNPdbe	rs794728508
MSV3d	rs794728508
GWAS Ctlg	rs794728508

Max Magnitude

5

ClinVar
Risk	rs794728508(-;-)
Alt	rs794728508(-;-)
Reference	Rs794728508(T;T)
Significance	Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNH2
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000007.13:g.150671952delA
CLNSRC
CLNACC	RCV000182068.1,