Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10410544 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1876828 0.851 0.160 17 45834159 intron variant C/T snv 0.14 4
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272