rs1060500628

Orientation

plus

Stabilized

plus

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

Make rs1060500628(G;T)

Make rs1060500628(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

2572062

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs1060500628
dbSNP (classic)	rs1060500628
ClinGen	rs1060500628
ebi	rs1060500628
HLI	rs1060500628
Exac	rs1060500628
Gnomad	rs1060500628
Varsome	rs1060500628
LitVar	rs1060500628
Map	rs1060500628
PheGenI	rs1060500628
Biobank	rs1060500628
1000 genomes	rs1060500628
hgdp	rs1060500628
ensembl	rs1060500628
geneview	rs1060500628
scholar	rs1060500628
google	rs1060500628
pharmgkb	rs1060500628
gwascentral	rs1060500628
openSNP	rs1060500628
23andMe	rs1060500628
SNPshot	rs1060500628
SNPdbe	rs1060500628
MSV3d	rs1060500628
GWAS Ctlg	rs1060500628

Max Magnitude

0

ClinVar
Risk	rs1060500628(T;T)
Alt	rs1060500628(T;T)
Reference	Rs1060500628(G;G)
Significance	Pathogenic
Disease	Long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2593292G>T
CLNSRC
CLNACC	RCV000459171.1,