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rs12205363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0
Make rs12205363(C;C)
Make rs12205363(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position129513484
GeneLAMA2
is asnp
is mentioned by
dbSNPrs12205363
ebirs12205363
HLIrs12205363
Exacrs12205363
Varsomers12205363
Maprs12205363
PheGenIrs12205363
hapmaprs12205363
1000 genomesrs12205363
hgdprs12205363
ensemblrs12205363
gopubmedrs12205363
geneviewrs12205363
scholarrs12205363
googlers12205363
pharmgkbrs12205363
gwascentralrs12205363
openSNPrs12205363
23andMers12205363
23andMe allrs12205363
SNP Nexus

SNPshotrs12205363
SNPdbers12205363
MSV3drs12205363
GWAS Ctlgrs12205363
GMAF0.03673
Max Magnitude0
? (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 C
P-val 2E-12
Odds Ratio .24 [0.17-0.3] unit increase

Occurs within the LAMA2 (Laminin alpha-2) gene