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rs7791362

From SNPedia

Orientationplus
Stabilizedplus
Make rs7791362(C;C)
Make rs7791362(C;T)
Make rs7791362(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position8103297
is asnp
is mentioned by
dbSNPrs7791362
ebirs7791362
HLIrs7791362
Exacrs7791362
Varsomers7791362
Maprs7791362
PheGenIrs7791362
hapmaprs7791362
1000 genomesrs7791362
hgdprs7791362
ensemblrs7791362
gopubmedrs7791362
geneviewrs7791362
scholarrs7791362
googlers7791362
pharmgkbrs7791362
gwascentralrs7791362
openSNPrs7791362
23andMers7791362
23andMe allrs7791362
SNP Nexus

SNPshotrs7791362
SNPdbers7791362
MSV3drs7791362
GWAS Ctlgrs7791362
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 C
P-val 4E-6
Odds Ratio 2.78 [1.62-3.94] unit decrease