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rs569688

From SNPedia

Orientationminus
Stabilizedminus
Make rs569688(A;A)
Make rs569688(A;C)
Make rs569688(C;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position60049262
is asnp
is mentioned by
dbSNPrs569688
ebirs569688
HLIrs569688
Exacrs569688
Varsomers569688
Maprs569688
PheGenIrs569688
hapmaprs569688
1000 genomesrs569688
hgdprs569688
ensemblrs569688
gopubmedrs569688
geneviewrs569688
scholarrs569688
googlers569688
pharmgkbrs569688
gwascentralrs569688
openSNPrs569688
23andMers569688
23andMe allrs569688
SNP Nexus

SNPshotrs569688
SNPdbers569688
MSV3drs569688
GWAS Ctlgrs569688
GMAF0.2612
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 4E-7
Odds Ratio NR NR