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rs12971120

From SNPedia

Orientationplus
Stabilizedplus
Make rs12971120(A;A)
Make rs12971120(A;G)
Make rs12971120(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position74506788
GeneCNDP2
is asnp
is mentioned by
dbSNPrs12971120
ebirs12971120
HLIrs12971120
Exacrs12971120
Varsomers12971120
Maprs12971120
PheGenIrs12971120
hapmaprs12971120
1000 genomesrs12971120
hgdprs12971120
ensemblrs12971120
gopubmedrs12971120
geneviewrs12971120
scholarrs12971120
googlers12971120
pharmgkbrs12971120
gwascentralrs12971120
openSNPrs12971120
23andMers12971120
23andMe allrs12971120
SNP Nexus

SNPshotrs12971120
SNPdbers12971120
MSV3drs12971120
GWAS Ctlgrs12971120
GMAF0.2043
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 2E-7
Odds Ratio .10 [0.062-0.136] unit increase