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rs7896005

From SNPedia

Orientationplus
Stabilizedplus
Make rs7896005(A;A)
Make rs7896005(A;G)
Make rs7896005(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position67891367
GeneSIRT1
is asnp
is mentioned by
dbSNPrs7896005
dbSNP (classic)rs7896005
ClinGenrs7896005
ebirs7896005
HLIrs7896005
Exacrs7896005
Gnomadrs7896005
Varsomers7896005
LitVarrs7896005
Maprs7896005
PheGenIrs7896005
Biobankrs7896005
1000 genomesrs7896005
hgdprs7896005
ensemblrs7896005
geneviewrs7896005
scholarrs7896005
googlers7896005
pharmgkbrs7896005
gwascentralrs7896005
openSNPrs7896005
23andMers7896005
SNPshotrs7896005
SNPdbers7896005
MSV3drs7896005
GWAS Ctlgrs7896005
GMAF0.3747
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21871827OA-icon.png] SIRT1 is associated with a decrease in acute insulin secretion and a sex specific increase in risk for type 2 diabetes in Pima Indians


[PMID 30393491OA-icon.png] Association of common polymorphisms in the VEGFA and SIRT1 genes with type 2 diabetes-related traits in Mexicans.


[PMID 30662452OA-icon.png] SIRT1 Allele Frequencies in Depressed Patients of European Descent in Russia.


[PMID 32967053OA-icon.png] SIRT1 Gene SNP rs932658 is Associated with Medication-Related Osteonecrosis of the Jaw.