Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7144658
TTC6 ; FOXA1
0.882 0.120 14 37592537 missense variant C/G;T snv 0.62 3
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs238417
ERCC2
1.000 0.080 19 45353210 intron variant G/C;T snv 0.59; 3.6E-05 1
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs2293152
STAT3
0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs1063499
C7
0.925 0.120 5 40955459 missense variant G/C snv 0.58 0.52 2
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs13332
CTSB
0.925 0.120 8 11849072 synonymous variant T/C;G snv 3.5E-02; 0.56 6
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 3
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2305619
VEPH1 ; PTX3
0.882 0.240 3 157437072 intron variant A/G snv 0.55 0.50 3
rs20575
TNFRSF10A
0.645 0.440 8 23201811 missense variant C/G snv 0.54 0.44 29
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1884444
IL23R ; C1orf141
0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1864183
ATG10
0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs1126497
EPCAM
0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1225944
TXNDC5 ; BLOC1S5-TXNDC5
1.000 0.080 6 7888855 splice region variant A/G snv 0.49 0.54 1
rs4147581
GSTP1
1.000 0.080 11 67584114 intron variant C/G snv 0.49 0.39 1
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131