Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs6682925 0.776 0.160 1 67165579 intron variant C/T snv 0.47 11
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs11564475 0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs4646421 0.882 0.080 15 74723851 intron variant G/A;C;T snv 0.21 3
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24