Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 32
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45