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rs2184971

From SNPedia

Orientationminus
Stabilizedminus
Make rs2184971(C;C)
Make rs2184971(C;T)
Make rs2184971(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position100165838
GenePCCA
is asnp
is mentioned by
dbSNPrs2184971
ebirs2184971
HLIrs2184971
Exacrs2184971
Varsomers2184971
Maprs2184971
PheGenIrs2184971
hapmaprs2184971
1000 genomesrs2184971
hgdprs2184971
ensemblrs2184971
gopubmedrs2184971
geneviewrs2184971
scholarrs2184971
googlers2184971
pharmgkbrs2184971
gwascentralrs2184971
openSNPrs2184971
23andMers2184971
23andMe allrs2184971
SNP Nexus

SNPshotrs2184971
SNPdbers2184971
MSV3drs2184971
GWAS Ctlgrs2184971
GMAF0.4486
Max Magnitude
? (C;C) (C;T) (T;T) 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-8
Odds Ratio .09 [0.056-0.114] unit increase