rs139042529

Orientation

plus

Stabilized

plus

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

Make rs139042529(C;T)

Make rs139042529(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2570663

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs139042529
dbSNP (classic)	rs139042529
ClinGen	rs139042529
ebi	rs139042529
HLI	rs139042529
Exac	rs139042529
Gnomad	rs139042529
Varsome	rs139042529
LitVar	rs139042529
Map	rs139042529
PheGenI	rs139042529
Biobank	rs139042529
1000 genomes	rs139042529
hgdp	rs139042529
ensembl	rs139042529
geneview	rs139042529
scholar	rs139042529
google	rs139042529
pharmgkb	rs139042529
gwascentral	rs139042529
openSNP	rs139042529
23andMe	rs139042529
SNPshot	rs139042529
SNPdbe	rs139042529
MSV3d	rs139042529
GWAS Ctlg	rs139042529

GMAF

0.0004591

Max Magnitude

0

ClinVar
Risk	rs139042529(A;A) rs139042529(G;G) rs139042529(T;T)
Alt	rs139042529(A;A) rs139042529(G;G) rs139042529(T;T)
Reference	Rs139042529(C;C)
Significance	Other
Disease	Long QT syndrome 1 Long QT syndrome not specified Cardiovascular phenotype Jervell and Lange-Nielsen syndrome Familial atrial fibrillation Short QT syndrome Romano-Ward syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome 1 Long QT syndrome not specified Cardiovascular phenotype Jervell and Lange-Nielsen syndrome Familial atrial fibrillation short QT syndrome Romano-Ward syndrome
Reversed	0
HGVS	NC_000011.9:g.2591893C>A; NC_000011.9:g.2591893C>G; NC_000011.9:g.2591893C>T
CLNSRC	ClinVar
CLNACC	RCV000477871.1, RCV000046070.3, RCV000155132.1, RCV000247674.1, RCV000268526.1, RCV000323618.1, RCV000326765.1, RCV000378309.1, RCV000381337.1,