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rs35706870

From SNPedia

Orientationplus
Stabilizedplus
Make rs35706870(A;A)
Make rs35706870(A;C)
Make rs35706870(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position67883859
GeneSIRT1
is asnp
is mentioned by
dbSNPrs35706870
ebirs35706870
HLIrs35706870
Exacrs35706870
Varsomers35706870
Maprs35706870
PheGenIrs35706870
hapmaprs35706870
1000 genomesrs35706870
hgdprs35706870
ensemblrs35706870
gopubmedrs35706870
geneviewrs35706870
scholarrs35706870
googlers35706870
pharmgkbrs35706870
gwascentralrs35706870
openSNPrs35706870
23andMers35706870
23andMe allrs35706870
SNP Nexus

SNPshotrs35706870
SNPdbers35706870
MSV3drs35706870
GWAS Ctlgrs35706870
Max Magnitude

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