rs1060500670

Orientation

minus

Stabilized

minus

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

Make rs1060500670(-;-)

Make rs1060500670(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150959642

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1060500670
dbSNP (classic)	rs1060500670
ClinGen	rs1060500670
ebi	rs1060500670
HLI	rs1060500670
Exac	rs1060500670
Gnomad	rs1060500670
Varsome	rs1060500670
LitVar	rs1060500670
Map	rs1060500670
PheGenI	rs1060500670
Biobank	rs1060500670
1000 genomes	rs1060500670
hgdp	rs1060500670
ensembl	rs1060500670
geneview	rs1060500670
scholar	rs1060500670
google	rs1060500670
pharmgkb	rs1060500670
gwascentral	rs1060500670
openSNP	rs1060500670
23andMe	rs1060500670
SNPshot	rs1060500670
SNPdbe	rs1060500670
MSV3d	rs1060500670
GWAS Ctlg	rs1060500670

Max Magnitude

0

ClinVar
Risk	rs1060500670(-;-)
Alt	rs1060500670(-;-)
Reference	Rs1060500670(G;G)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150656730delC
CLNSRC
CLNACC	RCV000477231.1,