Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs29001322 0.882 0.040 10 97462918 non coding transcript exon variant A/C;G snv 3
rs1057519736 0.752 0.160 15 90088605 missense variant C/G snv 13
rs199476133
ND3 ; COX3 ; ND4L ; ND4 ; ATP8 ; ATP6
0.742 0.320 MT 8993 missense variant T/C;G snv 18
rs1223868338 0.882 0.040 10 88990884 missense variant G/C snv 7.0E-06 3
rs10019009 0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1056629 0.827 0.120 16 82148499 3 prime UTR variant T/C snv 0.14 6
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs4778889 0.683 0.480 15 81296654 intron variant T/C snv 0.24 24
rs4072111 0.716 0.400 15 81285798 missense variant C/T snv 0.17 0.11 16
rs8064946 0.851 0.080 17 7685993 non coding transcript exon variant G/C snv 0.32 4
rs12602273 0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs1642785 0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05 6
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9895829 0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs876660254 0.882 0.040 17 7674963 missense variant G/T snv 4
rs1800372 0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs764146326 0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25