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rs7800418

From SNPedia

Orientationplus
Stabilizedplus
Make rs7800418(C;C)
Make rs7800418(C;T)
Make rs7800418(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position26566386
is asnp
is mentioned by
dbSNPrs7800418
ebirs7800418
HLIrs7800418
Exacrs7800418
Varsomers7800418
Maprs7800418
PheGenIrs7800418
hapmaprs7800418
1000 genomesrs7800418
hgdprs7800418
ensemblrs7800418
gopubmedrs7800418
geneviewrs7800418
scholarrs7800418
googlers7800418
pharmgkbrs7800418
gwascentralrs7800418
openSNPrs7800418
23andMers7800418
23andMe allrs7800418
SNP Nexus

SNPshotrs7800418
SNPdbers7800418
MSV3drs7800418
GWAS Ctlgrs7800418
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 T
P-val 7E-7
Odds Ratio 1.96 [1.20-2.73] unit decrease