Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs776223836 0.763 0.280 19 45364045 missense variant G/A snv 11
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1457582183 0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 5
rs1799966 0.807 0.280 17 43071077 missense variant T/A;C snv 5.2E-05; 0.35 8
rs1800372 0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs4796793 0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs7211777 0.882 0.120 17 42382057 intron variant G/A snv 0.52 3
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs781367751 0.851 0.200 17 34991822 missense variant A/G snv 1.2E-05 4
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs941759532 0.763 0.240 16 13932175 missense variant C/G snv 11
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10519097 0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1799814 0.807 0.160 15 74720646 missense variant G/A;T snv 1.6E-05; 3.1E-02 8
rs2602141 0.790 0.120 15 43432448 missense variant T/G snv 0.36 0.47 9
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs7164773 0.790 0.240 15 60775749 intron variant C/A;T snv 10
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55