rs569688

Orientation

minus

Stabilized

minus

Make rs569688(A;A)

Make rs569688(A;C)

Make rs569688(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

60049262

Gene	LOC105375861

is a	snp
is	mentioned by
dbSNP	rs569688
dbSNP (classic)	rs569688
ClinGen	rs569688
ebi	rs569688
HLI	rs569688
Exac	rs569688
Gnomad	rs569688
Varsome	rs569688
LitVar	rs569688
Map	rs569688
PheGenI	rs569688
Biobank	rs569688
1000 genomes	rs569688
hgdp	rs569688
ensembl	rs569688
geneview	rs569688
scholar	rs569688
google	rs569688
pharmgkb	rs569688
gwascentral	rs569688
openSNP	rs569688
23andMe	rs569688
SNPshot	rs569688
SNPdbe	rs569688
MSV3d	rs569688
GWAS Ctlg	rs569688

GMAF

0.2612

Max Magnitude

0

?	(A;A) (A;C) (C;C)	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-7
Odds Ratio	NR NR