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rs1585471

From SNPedia

Orientationplus
Stabilizedplus
Make rs1585471(A;A)
Make rs1585471(A;G)
Make rs1585471(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position111781479
is asnp
is mentioned by
dbSNPrs1585471
ebirs1585471
HLIrs1585471
Exacrs1585471
Varsomers1585471
Maprs1585471
PheGenIrs1585471
hapmaprs1585471
1000 genomesrs1585471
hgdprs1585471
ensemblrs1585471
gopubmedrs1585471
geneviewrs1585471
scholarrs1585471
googlers1585471
pharmgkbrs1585471
gwascentralrs1585471
openSNPrs1585471
23andMers1585471
23andMe allrs1585471
SNP Nexus

SNPshotrs1585471
SNPdbers1585471
MSV3drs1585471
GWAS Ctlgrs1585471
GMAF0.3503
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21505071]
Trait
Title A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.
Risk Allele
P-val 0.000002
Odds Ratio 1.1500 [1.09-1.22]


[PMID 22150588] Common variants in chromosome 4q25 are associated with myopia in Chinese adults.