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rs3138144

From SNPedia

Orientationminus
Stabilizedminus
Make rs3138144(C;C)
Make rs3138144(C;G)
Make rs3138144(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position55720985
GeneRDH5, RPL12P34
is asnp
is mentioned by
dbSNPrs3138144
ebirs3138144
HLIrs3138144
Exacrs3138144
Varsomers3138144
Maprs3138144
PheGenIrs3138144
hapmaprs3138144
1000 genomesrs3138144
hgdprs3138144
ensemblrs3138144
gopubmedrs3138144
geneviewrs3138144
scholarrs3138144
googlers3138144
pharmgkbrs3138144
gwascentralrs3138144
openSNPrs3138144
23andMers3138144
23andMe allrs3138144
SNP Nexus

SNPshotrs3138144
SNPdbers3138144
MSV3drs3138144
GWAS Ctlgrs3138144
GMAF0.3714
Max Magnitude
? (C;C) (C;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 C
P-val 4E-12
Odds Ratio .12 [0.086-0.152] unit increase


[PMID 20668683OA-icon.png] Genetically dependent ERBB3 expression modulates antigen presenting cell function and type 1 diabetes risk.