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rs17244419

From SNPedia

Orientationplus
Stabilizedplus
Make rs17244419(C;C)
Make rs17244419(C;T)
Make rs17244419(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position96704738
is asnp
is mentioned by
dbSNPrs17244419
ebirs17244419
HLIrs17244419
Exacrs17244419
Varsomers17244419
Maprs17244419
PheGenIrs17244419
hapmaprs17244419
1000 genomesrs17244419
hgdprs17244419
ensemblrs17244419
gopubmedrs17244419
geneviewrs17244419
scholarrs17244419
googlers17244419
pharmgkbrs17244419
gwascentralrs17244419
openSNPrs17244419
23andMers17244419
23andMe allrs17244419
SNP Nexus

SNPshotrs17244419
SNPdbers17244419
MSV3drs17244419
GWAS Ctlgrs17244419
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 8E-6
Odds Ratio 8.65 [4.89-12.41] unit decrease