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rs16953622

From SNPedia

Orientationplus
Stabilizedplus
Make rs16953622(C;C)
Make rs16953622(C;T)
Make rs16953622(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position96856485
is asnp
is mentioned by
dbSNPrs16953622
ebirs16953622
HLIrs16953622
Exacrs16953622
Varsomers16953622
Maprs16953622
PheGenIrs16953622
hapmaprs16953622
1000 genomesrs16953622
hgdprs16953622
ensemblrs16953622
gopubmedrs16953622
geneviewrs16953622
scholarrs16953622
googlers16953622
pharmgkbrs16953622
gwascentralrs16953622
openSNPrs16953622
23andMers16953622
23andMe allrs16953622
SNP Nexus

SNPshotrs16953622
SNPdbers16953622
MSV3drs16953622
GWAS Ctlgrs16953622
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-6
Odds Ratio 6.99 [3.97-10.01] unit decrease