Have questions? Visit https://www.reddit.com/r/SNPedia

rs7084402

From SNPedia

Orientationplus
Stabilizedplus
Make rs7084402(A;A)
Make rs7084402(A;G)
Make rs7084402(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position58505644
is asnp
is mentioned by
dbSNPrs7084402
ebirs7084402
HLIrs7084402
Exacrs7084402
Varsomers7084402
Maprs7084402
PheGenIrs7084402
hapmaprs7084402
1000 genomesrs7084402
hgdprs7084402
ensemblrs7084402
gopubmedrs7084402
geneviewrs7084402
scholarrs7084402
googlers7084402
pharmgkbrs7084402
gwascentralrs7084402
openSNPrs7084402
23andMers7084402
23andMe allrs7084402
SNP Nexus

SNPshotrs7084402
SNPdbers7084402
MSV3drs7084402
GWAS Ctlgrs7084402
GMAF0.4959
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 2E-13
Odds Ratio .11 [0.079-0.137] unit decrease