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

rs9307551

From SNPedia

Orientationplus
Stabilizedplus
Make rs9307551(A;A)
Make rs9307551(A;C)
Make rs9307551(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position79609517
is asnp
is mentioned by
dbSNPrs9307551
ebirs9307551
HLIrs9307551
Exacrs9307551
Varsomers9307551
Maprs9307551
PheGenIrs9307551
hapmaprs9307551
1000 genomesrs9307551
hgdprs9307551
ensemblrs9307551
gopubmedrs9307551
geneviewrs9307551
scholarrs9307551
googlers9307551
pharmgkbrs9307551
gwascentralrs9307551
openSNPrs9307551
23andMers9307551
23andMe allrs9307551
SNP Nexus

SNPshotrs9307551
SNPdbers9307551
MSV3drs9307551
GWAS Ctlgrs9307551
GMAF0.259
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 1E-8
Odds Ratio .10 [0.066-0.132] unit decrease

[PMID 25628894OA-icon.png] Evaluation of four genetic variants in han chinese subjects with high myopia