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rs6885224

From SNPedia

Orientationplus
Stabilizedplus
Make rs6885224(C;C)
Make rs6885224(C;T)
Make rs6885224(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position11169833
GeneCTNND2
is asnp
is mentioned by
dbSNPrs6885224
ebirs6885224
HLIrs6885224
Exacrs6885224
Varsomers6885224
Maprs6885224
PheGenIrs6885224
hapmaprs6885224
1000 genomesrs6885224
hgdprs6885224
ensemblrs6885224
gopubmedrs6885224
geneviewrs6885224
scholarrs6885224
googlers6885224
pharmgkbrs6885224
gwascentralrs6885224
openSNPrs6885224
23andMers6885224
23andMe allrs6885224
SNP Nexus

SNPshotrs6885224
SNPdbers6885224
MSV3drs6885224
GWAS Ctlgrs6885224
GMAF0.3471
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21095009OA-icon.png]
Trait
Title Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese
Risk Allele C
P-val 0.000008
Odds Ratio 1.2400 [1.11-1.39]


[PMID 21911587] Replication study supports CTNND2 as a susceptibility gene for high myopia.