Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 42
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 21
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs199476133
ND3 ; COX3 ; ND4L ; ND4 ; ATP8 ; ATP6
0.742 0.320 MT 8993 missense variant T/C;G snv 14
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs1554887097 0.807 0.320 10 100989331 missense variant G/A snv 10
rs113994096 0.827 0.080 15 89325639 missense variant G/A snv 1.5E-03 1.6E-03 7
rs121918054 0.807 0.240 15 89323460 missense variant C/G;T snv 6.9E-04; 4.0E-06 7
rs80356529 0.827 0.240 3 193643996 missense variant G/A;C snv 5
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 5
rs118192098
TRNK ; COX3 ; COX2 ; ATP6 ; ATP8 ; ND3
0.851 0.200 MT 8344 non coding transcript exon variant A/G snv 5
rs28937590 0.807 0.360 2 218661219 missense variant A/G snv 4.7E-04 4.1E-04 4
rs267606897
CYTB ; ND5
0.882 0.200 MT 13513 missense variant G/A snv 4
rs199476138
ND3 ; COX3 ; ND4 ; ND4L ; ATP6
0.882 0.120 MT 9185 missense variant T/C snv 4
rs80356530 0.882 0.320 3 193667168 splice region variant TTAG/- delins 4
rs886041081 0.925 4 185144891 missense variant G/A snv 4
rs121434453
TRNE ; ND6 ; CYTB
0.882 0.320 MT 14709 non coding transcript exon variant T/C snv 4
rs387906421
CYTB ; TRNE ; ND6
0.925 0.200 MT 14674 non coding transcript exon variant T/C;G snv 3
rs398124298 0.925 0.160 3 193647110 missense variant C/A;G snv 3
rs143319805 0.807 0.320 3 193643378 missense variant A/G snv 6.2E-04 5.7E-04 3
rs113994099 0.827 0.240 15 89320883 missense variant T/C snv 3
rs1131691575 0.925 0.080 15 89317469 missense variant C/T snv 8.0E-06 1.4E-05 3
rs115079861 1.000 6 151405236 stop lost C/G;T snv 2.0E-05; 4.0E-03 3
rs121908572 0.882 0.280 2 218661283 missense variant C/T snv 3
rs1555745989 0.925 0.040 19 1244118 missense variant T/G snv 2