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rs634990

From SNPedia

Orientationminus
Stabilizedminus
Make rs634990(A;A)
Make rs634990(A;G)
Make rs634990(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position34713872
is asnp
is mentioned by
dbSNPrs634990
ebirs634990
HLIrs634990
Exacrs634990
Varsomers634990
Maprs634990
PheGenIrs634990
hapmaprs634990
1000 genomesrs634990
hgdprs634990
ensemblrs634990
gopubmedrs634990
geneviewrs634990
scholarrs634990
googlers634990
pharmgkbrs634990
gwascentralrs634990
openSNPrs634990
23andMers634990
23andMe allrs634990
SNP Nexus

SNPshotrs634990
SNPdbers634990
MSV3drs634990
GWAS Ctlgrs634990
GMAF0.4826
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20835239OA-icon.png]
Trait
Title A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Risk Allele C
P-val 2E-14
Odds Ratio 0.23 [0.228-0.232] diopter increase


[PMID 22665138OA-icon.png] Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium


[PMID 21436269] Association of 15q14 and 15q25 with high myopia in Japanese.


[PMID 23131718] Genetic Association of Refractive Error and Axial Length with 15q14 but Not 15q25 in the Blue Mountains Eye Study Cohort