rs10747502

Orientation

plus

Stabilized

plus

Make rs10747502(A;A)

Make rs10747502(A;G)

Make rs10747502(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

99058491

Gene	LOC100129620

is a	snp
is	mentioned by
dbSNP	rs10747502
dbSNP (classic)	rs10747502
ClinGen	rs10747502
ebi	rs10747502
HLI	rs10747502
Exac	rs10747502
Gnomad	rs10747502
Varsome	rs10747502
LitVar	rs10747502
Map	rs10747502
PheGenI	rs10747502
Biobank	rs10747502
1000 genomes	rs10747502
hgdp	rs10747502
ensembl	rs10747502
geneview	rs10747502
scholar	rs10747502
google	rs10747502
pharmgkb	rs10747502
gwascentral	rs10747502
openSNP	rs10747502
23andMe	rs10747502
SNPshot	rs10747502
SNPdbe	rs10747502
MSV3d	rs10747502
GWAS Ctlg	rs10747502

GMAF

0.112

Max Magnitude

0

?	(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	1E-9
Odds Ratio	NR NR

GWAS snp
PMID	[PMID 23251661]
Trait	Obesity-related traits
Title	Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Risk Allele	A
P-val	5E-7
Odds Ratio	.04 [NR] %awake time increase