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rs12788764

From SNPedia

Orientationplus
Stabilizedplus
Make rs12788764(C;C)
Make rs12788764(C;T)
Make rs12788764(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position25112998
is asnp
is mentioned by
dbSNPrs12788764
ebirs12788764
HLIrs12788764
Exacrs12788764
Varsomers12788764
Maprs12788764
PheGenIrs12788764
hapmaprs12788764
1000 genomesrs12788764
hgdprs12788764
ensemblrs12788764
gopubmedrs12788764
geneviewrs12788764
scholarrs12788764
googlers12788764
pharmgkbrs12788764
gwascentralrs12788764
openSNPrs12788764
23andMers12788764
23andMe allrs12788764
SNP Nexus

SNPshotrs12788764
SNPdbers12788764
MSV3drs12788764
GWAS Ctlgrs12788764
Max Magnitude
GWAS snp
PMID [PMID 24951543]
Trait Age-related nuclear cataracts
Title Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.
Risk Allele C
P-val 5E-6
Odds Ratio .07 [0.05-0.09] unit decrease