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rs7849581

From SNPedia

Orientationplus
Stabilizedplus
Make rs7849581(C;C)
Make rs7849581(C;T)
Make rs7849581(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome9
Position9924724
GenePTPRD
is asnp
is mentioned by
dbSNPrs7849581
ebirs7849581
HLIrs7849581
Exacrs7849581
Varsomers7849581
Maprs7849581
PheGenIrs7849581
hapmaprs7849581
1000 genomesrs7849581
hgdprs7849581
ensemblrs7849581
gopubmedrs7849581
geneviewrs7849581
scholarrs7849581
googlers7849581
pharmgkbrs7849581
gwascentralrs7849581
openSNPrs7849581
23andMers7849581
23andMe allrs7849581
SNP Nexus

SNPshotrs7849581
SNPdbers7849581
MSV3drs7849581
GWAS Ctlgrs7849581
GMAF0.241
Max Magnitude
? (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