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
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
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
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs11119608 0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936 0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs11200014 0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
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
rs115392158 0.708 0.280 6 31347004 intron variant A/G snv 17
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55