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
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs765660823 0.882 0.200 1 162778720 missense variant A/C snv 1.9E-04 4
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1048638
CA9
0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 10
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs2299939 0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs754332870 0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs12108497 0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55