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rs4778879

From SNPedia

Orientationplus
Stabilizedplus
Make rs4778879(A;A)
Make rs4778879(A;G)
Make rs4778879(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position79080533
GeneRASGRF1
is asnp
is mentioned by
dbSNPrs4778879
ebirs4778879
HLIrs4778879
Exacrs4778879
Varsomers4778879
Maprs4778879
PheGenIrs4778879
hapmaprs4778879
1000 genomesrs4778879
hgdprs4778879
ensemblrs4778879
gopubmedrs4778879
geneviewrs4778879
scholarrs4778879
googlers4778879
pharmgkbrs4778879
gwascentralrs4778879
openSNPrs4778879
23andMers4778879
23andMe allrs4778879
SNP Nexus

SNPshotrs4778879
SNPdbers4778879
MSV3drs4778879
GWAS Ctlgrs4778879
GMAF0.4513
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 4E-11
Odds Ratio .10 [0.073-0.131] unit decrease