Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs2239704 0.732 0.320 6 31572364 5 prime UTR variant A/C snv 0.64 17
rs4968451 0.732 0.160 17 61849946 intron variant A/C snv 0.15 13
rs4652 0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs213210 0.742 0.240 6 33208047 upstream gene variant A/C;G snv 11
rs9298814 0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs3809728 0.851 0.120 17 12019847 intron 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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16