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rs12032643

From SNPedia

Orientationplus
Stabilizedplus
Make rs12032643(A;A)
Make rs12032643(A;G)
Make rs12032643(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position248874237
GenePGBD2
is asnp
is mentioned by
dbSNPrs12032643
dbSNP (classic)rs12032643
ClinGenrs12032643
ebirs12032643
HLIrs12032643
Exacrs12032643
Gnomadrs12032643
Varsomers12032643
LitVarrs12032643
Maprs12032643
PheGenIrs12032643
Biobankrs12032643
1000 genomesrs12032643
hgdprs12032643
ensemblrs12032643
geneviewrs12032643
scholarrs12032643
googlers12032643
pharmgkbrs12032643
gwascentralrs12032643
openSNPrs12032643
23andMers12032643
SNPshotrs12032643
SNPdbers12032643
MSV3drs12032643
GWAS Ctlgrs12032643
GMAF0.1827
Max Magnitude0
? (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 1E-9
Odds Ratio NR NR