rs2394443
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2394443(C;C) |
Make rs2394443(C;G) |
Make rs2394443(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 67884583 |
Gene | SIRT1 |
is a | snp |
is | mentioned by |
dbSNP | rs2394443 |
dbSNP (classic) | rs2394443 |
ClinGen | rs2394443 |
ebi | rs2394443 |
HLI | rs2394443 |
Exac | rs2394443 |
Gnomad | rs2394443 |
Varsome | rs2394443 |
LitVar | rs2394443 |
Map | rs2394443 |
PheGenI | rs2394443 |
Biobank | rs2394443 |
1000 genomes | rs2394443 |
hgdp | rs2394443 |
ensembl | rs2394443 |
geneview | rs2394443 |
scholar | rs2394443 |
rs2394443 | |
pharmgkb | rs2394443 |
gwascentral | rs2394443 |
openSNP | rs2394443 |
23andMe | rs2394443 |
SNPshot | rs2394443 |
SNPdbe | rs2394443 |
MSV3d | rs2394443 |
GWAS Ctlg | rs2394443 |
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.