Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs2273773
SIRT1
0.790 0.360 10 67906841 synonymous variant T/C snv 0.11 7.1E-02 9
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs10509291 0.827 0.280 10 67875446 downstream gene variant T/A snv 7.1E-02 6
rs3818292
SIRT1
0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 5
rs587777006
ERF
0.882 0.080 19 42249565 stop gained G/A;C snv 4.0E-06 3
rs33957861
SIRT1
0.882 0.160 10 67887218 intron variant C/T snv 0.11 3
rs587777007
ERF
0.925 0.080 19 42249220 frameshift variant CT/- del 2
rs3740051
SIRT1
0.925 0.200 10 67884201 upstream gene variant A/G;T snv 2
rs932658
SIRT1
0.925 0.120 10 67884459 upstream gene variant A/C;T snv 2
rs1085307555
TWIST1
0.925 0.080 7 19116993 missense variant C/G;T snv 2
rs121909188
TWIST1
0.925 0.080 7 19116946 stop gained C/A snv 2
rs1554441991
TWIST1
0.925 0.080 7 19116905 inframe insertion -/GGCAGCGTGGGGATGATCTTC delins 2
rs1554441993
TWIST1
0.925 0.080 7 19116913 frameshift variant -/G delins 2
rs1554441995
TWIST1
0.925 0.080 7 19116927 missense variant C/G snv 2
rs1554442019
TWIST1
0.925 0.080 7 19116976 missense variant G/C snv 2
rs1554442082
TWIST1
0.925 0.080 7 19117180 frameshift variant CGCGCTGCGCC/- delins 2
rs1563159980
TWIST1
0.925 0.080 7 19116903 stop gained -/AGGGCAGCGTGGGGATGATCT delins 2
rs1563160116
TWIST1
0.925 0.080 7 19117021 stop gained G/A snv 2
rs1563160337
TWIST1
0.925 0.080 7 19117211 frameshift variant CGTCCCCCGCGCTTGCCGCTCG/- delins 2
rs1555750741
ERF
1.000 0.080 19 42249379 frameshift variant G/- delins 1
rs1555750795
ERF
1.000 0.080 19 42249493 stop gained G/A snv 1
rs1555750816
ERF
1.000 0.080 19 42249545 frameshift variant CA/- delins 1
rs1568472771
ERF
1.000 0.080 19 42250365 stop gained G/A snv 1