Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28358278
ND3 ; ND4L ; ND5 ; COX3 ; ND4
0.925 0.080 MT 10400 synonymous variant C/T snv 2
rs2853826
ND4L ; COX3 ; ND5 ; ND3 ; ND4
0.925 0.080 MT 10398 missense variant A/G snv 2
rs41467651
ND4L ; ND4 ; COX3 ; ND3
0.925 0.080 MT 10310 synonymous variant G/A snv 2
rs1048369 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs111638916 0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs3747093 0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 16
rs17728461 0.776 0.120 22 30202563 intron variant C/G snv 0.25 9
rs12537 0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs5999749 0.925 0.080 22 21833371 intron variant A/C;T snv 3
rs775144154 0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs4819388 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs113593938 0.790 0.200 21 44250907 missense variant C/T snv 3.5E-03 7
rs4998557 0.851 0.080 21 31662579 intron variant G/A snv 0.22 4
rs184432 0.882 0.120 21 42367453 upstream gene variant G/A snv 0.64 3
rs225359 0.882 0.120 21 42367327 upstream gene variant G/A snv 0.62 3
rs3761376 0.925 0.080 21 42366929 upstream gene variant G/A snv 0.27 3
rs3814896 0.882 0.080 21 42351602 upstream gene variant A/G snv 0.17 3
rs9981660 0.882 0.080 21 42317828 upstream gene variant G/A snv 0.11 3
rs11088680 0.925 0.080 21 13514758 upstream gene variant A/G snv 0.30 2
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18