Have questions? Visit https://www.reddit.com/r/SNPedia

rs932658

From SNPedia

Orientationminus
Stabilizedminus
Make rs932658(G;G)
Make rs932658(G;T)
Make rs932658(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position67884459
GeneSIRT1
is asnp
is mentioned by
dbSNPrs932658
dbSNP (classic)rs932658
ClinGenrs932658
ebirs932658
HLIrs932658
Exacrs932658
Gnomadrs932658
Varsomers932658
LitVarrs932658
Maprs932658
PheGenIrs932658
Biobankrs932658
1000 genomesrs932658
hgdprs932658
ensemblrs932658
geneviewrs932658
scholarrs932658
googlers932658
pharmgkbrs932658
gwascentralrs932658
openSNPrs932658
23andMers932658
SNPshotrs932658
SNPdbers932658
MSV3drs932658
GWAS Ctlgrs932658
Max Magnitude0

[PMID 24875419] Functional sequence variants within the SIRT1 gene promoter in indirect inguinal hernia


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