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rs17788937

From SNPedia

Orientationplus
Stabilizedplus
Make rs17788937(A;A)
Make rs17788937(A;G)
Make rs17788937(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position77505730
GeneNAV3
is asnp
is mentioned by
dbSNPrs17788937
ebirs17788937
HLIrs17788937
Exacrs17788937
Varsomers17788937
Maprs17788937
PheGenIrs17788937
hapmaprs17788937
1000 genomesrs17788937
hgdprs17788937
ensemblrs17788937
gopubmedrs17788937
geneviewrs17788937
scholarrs17788937
googlers17788937
pharmgkbrs17788937
gwascentralrs17788937
openSNPrs17788937
23andMers17788937
23andMe allrs17788937
SNP Nexus

SNPshotrs17788937
SNPdbers17788937
MSV3drs17788937
GWAS Ctlgrs17788937
GMAF0.1166
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 4E-15
Odds Ratio NR NR