rs7849581

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs7849581(C;T)

Make rs7849581(T;T)

Reference

GRCh37.p5 37.3/137

Chromosome

9

Position

9924724

Gene

PTPRD

is a	snp
is	mentioned by
dbSNP	rs7849581
dbSNP (classic)	rs7849581
ClinGen	rs7849581
ebi	rs7849581
HLI	rs7849581
Exac	rs7849581
Gnomad	rs7849581
Varsome	rs7849581
LitVar	rs7849581
Map	rs7849581
PheGenI	rs7849581
Biobank	rs7849581
1000 genomes	rs7849581
hgdp	rs7849581
ensembl	rs7849581
geneview	rs7849581
scholar	rs7849581
google	rs7849581
pharmgkb	rs7849581
gwascentral	rs7849581
openSNP	rs7849581
23andMe	rs7849581
SNPshot	rs7849581
SNPdbe	rs7849581
MSV3d	rs7849581
GWAS Ctlg	rs7849581

GMAF

0.241

Max Magnitude

0

?	(C;C) (C;T) (T;T)	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	9E-7
Odds Ratio	NR NR