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rs7945071

From SNPedia

Orientationplus
Stabilizedplus
Make rs7945071(G;G)
Make rs7945071(G;T)
Make rs7945071(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position110373198
is asnp
is mentioned by
dbSNPrs7945071
ebirs7945071
HLIrs7945071
Exacrs7945071
Varsomers7945071
Maprs7945071
PheGenIrs7945071
hapmaprs7945071
1000 genomesrs7945071
hgdprs7945071
ensemblrs7945071
gopubmedrs7945071
geneviewrs7945071
scholarrs7945071
googlers7945071
pharmgkbrs7945071
gwascentralrs7945071
openSNPrs7945071
23andMers7945071
23andMe allrs7945071
SNP Nexus

SNPshotrs7945071
SNPdbers7945071
MSV3drs7945071
GWAS Ctlgrs7945071
Max Magnitude
? (G;G) (G;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 T
P-val 7E-6
Odds Ratio 3.01 [1.71-4.31] unit increase