Have questions? Visit https://www.reddit.com/r/SNPedia

rs7215564

From SNPedia

Orientationplus
Stabilizedplus
Make rs7215564(C;C)
Make rs7215564(C;T)
Make rs7215564(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position80763487
GeneRPTOR
is asnp
is mentioned by
dbSNPrs7215564
ebirs7215564
HLIrs7215564
Exacrs7215564
Varsomers7215564
Maprs7215564
PheGenIrs7215564
hapmaprs7215564
1000 genomesrs7215564
hgdprs7215564
ensemblrs7215564
gopubmedrs7215564
geneviewrs7215564
scholarrs7215564
googlers7215564
pharmgkbrs7215564
gwascentralrs7215564
openSNPrs7215564
23andMers7215564
23andMe allrs7215564
SNP Nexus

SNPshotrs7215564
SNPdbers7215564
MSV3drs7215564
GWAS Ctlgrs7215564
GMAF0.1263
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 2E-6
Odds Ratio NR NR