rs4737395

Orientation

plus

Stabilized

plus

Make rs4737395(A;A)

Make rs4737395(A;G)

Make rs4737395(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

55686989

is a	snp
is	mentioned by
dbSNP	rs4737395
dbSNP (classic)	rs4737395
ClinGen	rs4737395
ebi	rs4737395
HLI	rs4737395
Exac	rs4737395
Gnomad	rs4737395
Varsome	rs4737395
LitVar	rs4737395
Map	rs4737395
PheGenI	rs4737395
Biobank	rs4737395
1000 genomes	rs4737395
hgdp	rs4737395
ensembl	rs4737395
geneview	rs4737395
scholar	rs4737395
google	rs4737395
pharmgkb	rs4737395
gwascentral	rs4737395
openSNP	rs4737395
23andMe	rs4737395
SNPshot	rs4737395
SNPdbe	rs4737395
MSV3d	rs4737395
GWAS Ctlg	rs4737395

GMAF

0.1263

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	5E-9
Odds Ratio	NR NR