rs7323755

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs7323755(A;A)

Make rs7323755(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

45326132

is a	snp
is	mentioned by
dbSNP	rs7323755
dbSNP (classic)	rs7323755
ClinGen	rs7323755
ebi	rs7323755
HLI	rs7323755
Exac	rs7323755
Gnomad	rs7323755
Varsome	rs7323755
LitVar	rs7323755
Map	rs7323755
PheGenI	rs7323755
Biobank	rs7323755
1000 genomes	rs7323755
hgdp	rs7323755
ensembl	rs7323755
geneview	rs7323755
scholar	rs7323755
google	rs7323755
pharmgkb	rs7323755
gwascentral	rs7323755
openSNP	rs7323755
23andMe	rs7323755
SNPshot	rs7323755
SNPdbe	rs7323755
MSV3d	rs7323755
GWAS Ctlg	rs7323755

GMAF

0.06107

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	2E-13
Odds Ratio	NR NR