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rs12216812

From SNPedia

Orientationplus
Stabilizedplus
Make rs12216812(A;A)
Make rs12216812(A;G)
Make rs12216812(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position81239512
is asnp
is mentioned by
dbSNPrs12216812
ebirs12216812
HLIrs12216812
Exacrs12216812
Varsomers12216812
Maprs12216812
PheGenIrs12216812
hapmaprs12216812
1000 genomesrs12216812
hgdprs12216812
ensemblrs12216812
gopubmedrs12216812
geneviewrs12216812
scholarrs12216812
googlers12216812
pharmgkbrs12216812
gwascentralrs12216812
openSNPrs12216812
23andMers12216812
23andMe allrs12216812
SNP Nexus

SNPshotrs12216812
SNPdbers12216812
MSV3drs12216812
GWAS Ctlgrs12216812
GMAF0.05005
Max Magnitude
? (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 3E-9
Odds Ratio NR NR