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rs2394443

From SNPedia

Orientationplus
Stabilizedplus
Make rs2394443(C;C)
Make rs2394443(C;G)
Make rs2394443(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position67884583
GeneSIRT1
is asnp
is mentioned by
dbSNPrs2394443
ebirs2394443
HLIrs2394443
Exacrs2394443
Varsomers2394443
Maprs2394443
PheGenIrs2394443
hapmaprs2394443
1000 genomesrs2394443
hgdprs2394443
ensemblrs2394443
gopubmedrs2394443
geneviewrs2394443
scholarrs2394443
googlers2394443
pharmgkbrs2394443
gwascentralrs2394443
openSNPrs2394443
23andMers2394443
23andMe allrs2394443
SNP Nexus

SNPshotrs2394443
SNPdbers2394443
MSV3drs2394443
GWAS Ctlgrs2394443
Max Magnitude

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