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rs2077233

From SNPedia

Orientationminus
Stabilizedminus
Make rs2077233(C;C)
Make rs2077233(C;T)
Make rs2077233(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position137182626
is asnp
is mentioned by
dbSNPrs2077233
ebirs2077233
HLIrs2077233
Exacrs2077233
Varsomers2077233
Maprs2077233
PheGenIrs2077233
hapmaprs2077233
1000 genomesrs2077233
hgdprs2077233
ensemblrs2077233
gopubmedrs2077233
geneviewrs2077233
scholarrs2077233
googlers2077233
pharmgkbrs2077233
gwascentralrs2077233
openSNPrs2077233
23andMers2077233
23andMe allrs2077233
SNP Nexus

SNPshotrs2077233
SNPdbers2077233
MSV3drs2077233
GWAS Ctlgrs2077233
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24684796OA-icon.png]
Trait Cognitive function
Title Heritability and genetic association analysis of cognition in the Diabetes Heart Study.
Risk Allele A
P-val 7E-6
Odds Ratio 2.31 [1.31-3.30] unit decrease