rs12803066

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	2.5	increased risk of myopia

Make rs12803066(A;A)

Make rs12803066(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

100172688

Gene

CNTN5

is a	snp
is	mentioned by
dbSNP	rs12803066
dbSNP (classic)	rs12803066
ClinGen	rs12803066
ebi	rs12803066
HLI	rs12803066
Exac	rs12803066
Gnomad	rs12803066
Varsome	rs12803066
LitVar	rs12803066
Map	rs12803066
PheGenI	rs12803066
Biobank	rs12803066
1000 genomes	rs12803066
hgdp	rs12803066
ensembl	rs12803066
geneview	rs12803066
scholar	rs12803066
google	rs12803066
pharmgkb	rs12803066
gwascentral	rs12803066
openSNP	rs12803066
23andMe	rs12803066
SNPshot	rs12803066
SNPdbe	rs12803066
MSV3d	rs12803066
GWAS Ctlg	rs12803066

GMAF

0.1442

Max Magnitude

2.5

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 23049088]
Trait	Myopia (pathological)
Title	A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val	4E-6
Odds Ratio	NR NR