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rs3741489

From SNPedia

Orientationplus
Stabilizedplus
Make rs3741489(C;C)
Make rs3741489(C;T)
Make rs3741489(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position132841216
GeneCHFR
is asnp
is mentioned by
dbSNPrs3741489
ebirs3741489
HLIrs3741489
Exacrs3741489
Varsomers3741489
Maprs3741489
PheGenIrs3741489
hapmaprs3741489
1000 genomesrs3741489
hgdprs3741489
ensemblrs3741489
gopubmedrs3741489
geneviewrs3741489
scholarrs3741489
googlers3741489
pharmgkbrs3741489
gwascentralrs3741489
openSNPrs3741489
23andMers3741489
23andMe allrs3741489
SNP Nexus

SNPshotrs3741489
SNPdbers3741489
MSV3drs3741489
GWAS Ctlgrs3741489
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 2E-6
Odds Ratio 13.94 [8.26-19.61] unit decrease