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rs931317

From SNPedia

Orientationplus
Stabilizedplus
Make rs931317(A;A)
Make rs931317(A;G)
Make rs931317(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position59943125
GeneFHIT
is asnp
is mentioned by
dbSNPrs931317
ebirs931317
HLIrs931317
Exacrs931317
Varsomers931317
Maprs931317
PheGenIrs931317
hapmaprs931317
1000 genomesrs931317
hgdprs931317
ensemblrs931317
gopubmedrs931317
geneviewrs931317
scholarrs931317
googlers931317
pharmgkbrs931317
gwascentralrs931317
openSNPrs931317
23andMers931317
23andMe allrs931317
SNP Nexus

SNPshotrs931317
SNPdbers931317
MSV3drs931317
GWAS Ctlgrs931317
GMAF0.1726
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-6
Odds Ratio NR NR