rs3818292, SIRT1

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Craniosynostosis, Type 1
CUI: C4551902
Disease: Craniosynostosis, Type 1
28 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 0.010 1.000 1 2019 2019
Diabetic Nephropathy
CUI: C0011881
Disease: Diabetic Nephropathy
238 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 0.010 1.000 1 2018 2018
Kidney Calculi
CUI: C0022650
Disease: Kidney Calculi
71 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 0.010 1 2015 2015
Nephrolithiasis
CUI: C0392525
Disease: Nephrolithiasis
99 0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 0.010 1.000 1 2019 2019