Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799930 0.716 0.400 8 18400593 missense variant G/A snv 0.27 0.27 17
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs2228000
XPC
0.585 0.560 3 14158387 missense variant G/A snv 0.24 0.21 53
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 36
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 37
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 39
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs376040996
XPA
0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 153