rs999556

Orientation

plus

Stabilized

plus

Make rs999556(A;A)

Make rs999556(A;G)

Make rs999556(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

151094113

is a	snp
is	mentioned by
dbSNP	rs999556
dbSNP (classic)	rs999556
ClinGen	rs999556
ebi	rs999556
HLI	rs999556
Exac	rs999556
Gnomad	rs999556
Varsome	rs999556
LitVar	rs999556
Map	rs999556
PheGenI	rs999556
Biobank	rs999556
1000 genomes	rs999556
hgdp	rs999556
ensembl	rs999556
geneview	rs999556
scholar	rs999556
google	rs999556
pharmgkb	rs999556
gwascentral	rs999556
openSNP	rs999556
23andMe	rs999556
SNPshot	rs999556
SNPdbe	rs999556
MSV3d	rs999556
GWAS Ctlg	rs999556

GMAF

0.4775

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-15
Odds Ratio	NR NR