rs932658
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs932658(G;G) |
Make rs932658(G;T) |
Make rs932658(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 67884459 |
Gene | SIRT1 |
is a | snp |
is | mentioned by |
dbSNP | rs932658 |
dbSNP (classic) | rs932658 |
ClinGen | rs932658 |
ebi | rs932658 |
HLI | rs932658 |
Exac | rs932658 |
Gnomad | rs932658 |
Varsome | rs932658 |
LitVar | rs932658 |
Map | rs932658 |
PheGenI | rs932658 |
Biobank | rs932658 |
1000 genomes | rs932658 |
hgdp | rs932658 |
ensembl | rs932658 |
geneview | rs932658 |
scholar | rs932658 |
rs932658 | |
pharmgkb | rs932658 |
gwascentral | rs932658 |
openSNP | rs932658 |
23andMe | rs932658 |
SNPshot | rs932658 |
SNPdbe | rs932658 |
MSV3d | rs932658 |
GWAS Ctlg | rs932658 |
Max Magnitude | 0 |
[PMID 24875419] Functional sequence variants within the SIRT1 gene promoter in indirect inguinal hernia
[PMID 32967053] SIRT1 Gene SNP rs932658 is Associated with Medication-Related Osteonecrosis of the Jaw.