Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12443621 0.807 0.120 16 52514125 intron variant A/G snv 0.48 6
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1776148 0.807 0.160 1 241879243 missense variant A/G snv 0.66 0.66 9
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs34009635 0.716 0.360 11 102713445 missense variant A/G snv 2.5E-03 6.2E-04 17
rs3731239 0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3754093 0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs4809957 0.763 0.240 20 54154632 3 prime UTR variant A/G snv 0.29 10
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131