rs2270676

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs2270676(C;C)

Make rs2270676(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

74457366

Gene

KCNE3

is a	snp
is	mentioned by
dbSNP	rs2270676
dbSNP (classic)	rs2270676
ClinGen	rs2270676
ebi	rs2270676
HLI	rs2270676
Exac	rs2270676
Gnomad	rs2270676
Varsome	rs2270676
LitVar	rs2270676
Map	rs2270676
PheGenI	rs2270676
Biobank	rs2270676
1000 genomes	rs2270676
hgdp	rs2270676
ensembl	rs2270676
geneview	rs2270676
scholar	rs2270676
google	rs2270676
pharmgkb	rs2270676
gwascentral	rs2270676
openSNP	rs2270676
23andMe	rs2270676
SNPshot	rs2270676
SNPdbe	rs2270676
MSV3d	rs2270676
GWAS Ctlg	rs2270676

GMAF

0.1235

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22144915]
Trait
Title	Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism.
Risk Allele	G
P-val	0.000005
Odds Ratio	1.2900 None

ClinVar
Risk	rs2270676(C;C)
Alt	rs2270676(C;C)
Reference	Rs2270676(T;T)
Significance	Probable-non-pathogenic
Disease	Cardiovascular phenotype not specified Brugada syndrome
Variation	info
Gene	KCNE3
CLNDBN	Cardiovascular phenotype not specified Brugada syndrome
Reversed	1
HGVS	NC_000011.9:g.74168411A>G
CLNSRC
CLNACC	RCV000245979.1, RCV000250331.1, RCV000399032.1,