rs1060500661

Orientation

minus

Stabilized

minus

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

Make rs1060500661(-;-)

Make rs1060500661(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150951698

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1060500661
dbSNP (classic)	rs1060500661
ClinGen	rs1060500661
ebi	rs1060500661
HLI	rs1060500661
Exac	rs1060500661
Gnomad	rs1060500661
Varsome	rs1060500661
LitVar	rs1060500661
Map	rs1060500661
PheGenI	rs1060500661
Biobank	rs1060500661
1000 genomes	rs1060500661
hgdp	rs1060500661
ensembl	rs1060500661
geneview	rs1060500661
scholar	rs1060500661
google	rs1060500661
pharmgkb	rs1060500661
gwascentral	rs1060500661
openSNP	rs1060500661
23andMe	rs1060500661
SNPshot	rs1060500661
SNPdbe	rs1060500661
MSV3d	rs1060500661
GWAS Ctlg	rs1060500661

Max Magnitude

0

ClinVar
Risk	rs1060500661(-;-)
Alt	rs1060500661(-;-)
Reference	Rs1060500661(C;C)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648786delG
CLNSRC
CLNACC	RCV000470097.1,