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rs17183295

From SNPedia

Orientationplus
Stabilizedplus
Make rs17183295(C;C)
Make rs17183295(C;T)
Make rs17183295(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position32751254
GeneMYO1D
is asnp
is mentioned by
dbSNPrs17183295
ebirs17183295
HLIrs17183295
Exacrs17183295
Varsomers17183295
Maprs17183295
PheGenIrs17183295
hapmaprs17183295
1000 genomesrs17183295
hgdprs17183295
ensemblrs17183295
gopubmedrs17183295
geneviewrs17183295
scholarrs17183295
googlers17183295
pharmgkbrs17183295
gwascentralrs17183295
openSNPrs17183295
23andMers17183295
23andMe allrs17183295
SNP Nexus

SNPshotrs17183295
SNPdbers17183295
MSV3drs17183295
GWAS Ctlgrs17183295
GMAF0.0955
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele T
P-val 1E-10
Odds Ratio .13 [0.092-0.17] unit decrease