Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1202989817 0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs1204382931 0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54