rs1060500623

Orientation

plus

Stabilized

plus

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

Make rs1060500623(-;-)

Make rs1060500623(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

2445298

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs1060500623
dbSNP (classic)	rs1060500623
ClinGen	rs1060500623
ebi	rs1060500623
HLI	rs1060500623
Exac	rs1060500623
Gnomad	rs1060500623
Varsome	rs1060500623
LitVar	rs1060500623
Map	rs1060500623
PheGenI	rs1060500623
Biobank	rs1060500623
1000 genomes	rs1060500623
hgdp	rs1060500623
ensembl	rs1060500623
geneview	rs1060500623
scholar	rs1060500623
google	rs1060500623
pharmgkb	rs1060500623
gwascentral	rs1060500623
openSNP	rs1060500623
23andMe	rs1060500623
SNPshot	rs1060500623
SNPdbe	rs1060500623
MSV3d	rs1060500623
GWAS Ctlg	rs1060500623

Max Magnitude

0

ClinVar
Risk	rs1060500623(-;-)
Alt	rs1060500623(-;-)
Reference	Rs1060500623(C;C)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2466528delC
CLNSRC
CLNACC	RCV000458842.1,