Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2239704 0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 16
rs765660823 0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs1131691021 0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs967461896 0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs587782289 0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1397529 0.882 0.080 4 143471009 3 prime UTR variant A/C;T snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs746284240 0.763 0.240 12 68809243 missense variant A/G snv 11
rs33917957
MET
0.790 0.120 7 116700208 missense variant A/G snv 2.7E-02 1.8E-02 10
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs1164376164 0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs2168351 0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730 0.851 0.120 15 92443898 intron variant A/G snv 0.44 6