Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507549 0.742 0.240 12 112489104 missense variant C/A;G snv 7
rs28384199
ND5 ; ND4
0.882 0.160 MT 11777 missense variant C/A;G snv 3
rs782609482 1.000 0.120 9 133352060 splice donor variant C/A;T snv 4.1E-06 4
rs1131692037 0.925 0.120 16 1773083 stop gained C/A;T snv 2
rs759452074 0.925 0.200 22 50523835 missense variant C/A;T snv 8.0E-06; 3.2E-05 2
rs1391748504 1.000 0.120 9 133352143 splice acceptor variant C/G snv 7.0E-06 1
rs863224926 1.000 0.120 9 133356268 splice donor variant C/G snv 1
rs28939714 0.882 0.160 11 47582140 missense variant C/G;T snv 4.0E-06 1
rs142441643 0.732 0.320 5 223509 stop gained C/T snv 2.0E-04 2.4E-04 12
rs113994098 0.742 0.320 15 89321792 missense variant C/T snv 1.5E-04 2.7E-04 10
rs762425351 0.925 0.200 9 129095573 missense variant C/T snv 1.2E-04 7.7E-05 7
rs137852863 0.882 0.120 5 61073136 stop gained C/T snv 4.0E-05 3.5E-05 5
rs121908576 0.851 0.360 2 218661153 stop gained C/T snv 1.7E-04 2.9E-04 4
rs199476144
ND1 ; TRNV
0.925 0.200 MT 1624 non coding transcript exon variant C/T snv 3
rs9809219 0.925 0.120 5 251100 missense variant C/T snv 4.0E-05 1.4E-05 3
rs137852767 0.925 0.120 5 251011 missense variant C/T snv 2
rs28933402 0.925 0.120 9 133353893 missense variant C/T snv 2
rs28939679 0.925 0.120 11 68033147 missense variant C/T snv 8.1E-06 2
rs104894270 0.882 0.160 11 47582436 missense variant C/T snv 1.6E-05 2.8E-05 1
rs1135402725 0.851 0.120 11 34995002 stop gained C/T snv 1.2E-05 1
rs113994093 1.000 0.120 15 89330241 missense variant C/T snv 1.2E-05 1.4E-05 1
rs782033035 1.000 0.120 9 133353894 missense variant C/T snv 1.2E-05 1
rs1554062427 1.000 0.120 5 53683163 frameshift variant CC/- del 1
rs782490558 0.882 0.120 9 133352101 frameshift variant CT/- delins 1.6E-05 3.5E-05 3
rs1554768333 1.000 0.120 9 133352565 frameshift variant CT/- delins 1