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rs16862782

From SNPedia

Orientationplus
Stabilizedplus
Make rs16862782(A;A)
Make rs16862782(A;C)
Make rs16862782(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position187970102
GeneRFX3
is asnp
is mentioned by
dbSNPrs16862782
ebirs16862782
HLIrs16862782
Exacrs16862782
Varsomers16862782
Maprs16862782
PheGenIrs16862782
hapmaprs16862782
1000 genomesrs16862782
hgdprs16862782
ensemblrs16862782
gopubmedrs16862782
geneviewrs16862782
scholarrs16862782
googlers16862782
pharmgkbrs16862782
gwascentralrs16862782
openSNPrs16862782
23andMers16862782
23andMe allrs16862782
SNP Nexus

SNPshotrs16862782
SNPdbers16862782
MSV3drs16862782
GWAS Ctlgrs16862782
GMAF0.1276
Max Magnitude
? (A;A) (A;C) (C;C) 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 5E-7
Odds Ratio NR NR