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rs1479617

From SNPedia

Orientationminus
Stabilizedminus
Make rs1479617(C;C)
Make rs1479617(C;T)
Make rs1479617(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position11386094
GeneCTNND2
is asnp
is mentioned by
dbSNPrs1479617
ebirs1479617
HLIrs1479617
Exacrs1479617
Varsomers1479617
Maprs1479617
PheGenIrs1479617
hapmaprs1479617
1000 genomesrs1479617
hgdprs1479617
ensemblrs1479617
gopubmedrs1479617
geneviewrs1479617
scholarrs1479617
googlers1479617
pharmgkbrs1479617
gwascentralrs1479617
openSNPrs1479617
23andMers1479617
23andMe allrs1479617
SNP Nexus

SNPshotrs1479617
SNPdbers1479617
MSV3drs1479617
GWAS Ctlgrs1479617
GMAF0.4063
Max Magnitude

[PMID 22759899] Polymorphisms in the CTNND2 gene and 11q24.1 genomic region are associated with pathological myopia in a Chinese population