Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs727502818 0.790 0.160 11 17772053 missense variant G/A snv 26
rs28933385 0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1135401778 0.752 0.400 17 67854315 frameshift variant T/- del 20
rs267606670 0.790 0.320 19 41968837 missense variant C/A;T snv 19
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs199476133
ND3 ; COX3 ; ND4L ; ND4 ; ATP8 ; ATP6
0.742 0.320 MT 8993 missense variant T/C;G snv 18
rs181109321 0.776 0.320 8 63065904 splice region variant C/A;T snv 2.0E-05 17
rs1057519429 0.807 0.240 19 13235666 missense variant C/G;T snv 15
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs672601370 0.790 0.160 2 240775863 missense variant G/A snv 13
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12
rs143319805 0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 12
rs1057520918 0.790 0.160 19 13262780 missense variant C/T snv 11
rs767181086 0.827 0.240 1 183220922 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs58982919 0.790 0.080 8 24956223 missense variant T/C snv 10
rs121908217 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 9
rs28933383 0.851 0.120 12 4912055 missense variant C/A;G;T snv 8
rs138249161 0.827 0.240 12 106432421 missense variant T/A snv 2.7E-04 3.0E-04 8