rs12038826

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs12038826(C;C)

Make rs12038826(C;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

230787205

Gene	CAPN9, LOC107985359

is a	snp
is	mentioned by
dbSNP	rs12038826
dbSNP (classic)	rs12038826
ClinGen	rs12038826
ebi	rs12038826
HLI	rs12038826
Exac	rs12038826
Gnomad	rs12038826
Varsome	rs12038826
LitVar	rs12038826
Map	rs12038826
PheGenI	rs12038826
Biobank	rs12038826
1000 genomes	rs12038826
hgdp	rs12038826
ensembl	rs12038826
geneview	rs12038826
scholar	rs12038826
google	rs12038826
pharmgkb	rs12038826
gwascentral	rs12038826
openSNP	rs12038826
23andMe	rs12038826
SNPshot	rs12038826
SNPdbe	rs12038826
MSV3d	rs12038826
GWAS Ctlg	rs12038826

GMAF

0.06749

Max Magnitude

0

?	(C;C) (C;T) (T;T)	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	7E-6
Odds Ratio	NR NR