rs11618212

Orientation

plus

Stabilized

plus

Make rs11618212(A;A)

Make rs11618212(A;G)

Make rs11618212(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

105444463

is a	snp
is	mentioned by
dbSNP	rs11618212
dbSNP (classic)	rs11618212
ClinGen	rs11618212
ebi	rs11618212
HLI	rs11618212
Exac	rs11618212
Gnomad	rs11618212
Varsome	rs11618212
LitVar	rs11618212
Map	rs11618212
PheGenI	rs11618212
Biobank	rs11618212
1000 genomes	rs11618212
hgdp	rs11618212
ensembl	rs11618212
geneview	rs11618212
scholar	rs11618212
google	rs11618212
pharmgkb	rs11618212
gwascentral	rs11618212
openSNP	rs11618212
23andMe	rs11618212
SNPshot	rs11618212
SNPdbe	rs11618212
MSV3d	rs11618212
GWAS Ctlg	rs11618212

GMAF

0.152

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-12
Odds Ratio	NR NR