Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434427
NDUFS2
0.923 0.036 1 161209912 missense variant G/A snp 2
rs121434428
NDUFS2
0.923 0.036 1 161209915 missense variant C/A snp 2
rs121434429
NDUFS2 ; FCER1G
0.923 0.036 1 161213673 missense variant T/C snp 2
rs142609245
NDUFB3
0.923 0.036 2 201078946 missense variant T/C snp 8.5E-04 8.0E-04 2
rs199422224
NDUFS1
0.923 0.036 2 206145009 missense variant T/C snp 4.0E-06 2
rs199422225
NDUFS1
0.923 0.036 2 206146919 missense variant G/A snp 2
rs121918134
DALRD3 ; MIR191 ; NDUFAF3
0.923 0.036 3 49022497 missense variant G/A,C snp 4.0E-06 2
rs121918135
NDUFAF3 ; DALRD3
0.923 0.036 3 49022903 missense variant G/C snp 2
rs267606913
NDUFS6
0.923 0.036 5 1815885 missense variant G/A snp 4.0E-06 2
rs63751061
KLHL32 ; NDUFAF4
0.923 0.036 6 96896790 missense variant A/G snp 2
rs1057519084
NDUFAF6
0.878 0.107 8 95032023 missense variant T/C snp 2
rs1057519085
NDUFAF6
0.878 0.107 8 95032003 missense variant A/T snp 2
rs1057519086
NDUFAF6
0.878 0.107 8 95052177 missense variant A/G snp 2
rs137853184
NDUFAF6
0.878 0.107 8 95032093 missense variant A/G snp 2
rs201732170
NDUFAF6
0.923 0.036 8 95035527 missense variant T/A,C snp 4.0E-06; 9.2E-05 3.2E-05 2
rs768273248
NDUFAF6
0.878 0.107 8 95048547 missense variant C/G,T snp 4.0E-06; 8.0E-06 2
rs121913660
NDUFV1
0.923 0.036 11 67611511 missense variant C/T snp 3.2E-05 3.2E-05 2
rs121913661
NDUFV1
0.923 0.036 11 67610510 missense variant G/A snp 3.2E-05 2
rs267606830
FOXRED1
0.923 0.036 11 126277517 missense variant A/C,G snp 4.0E-06 2
rs387907087
FOXRED1
0.923 0.036 11 126276476 missense variant C/T snp 2.4E-05 6.4E-05 2
rs397515440
NUBPL
0.923 0.036 14 31599310 missense variant G/T snp 2.0E-05 3.2E-05 2
rs552722349
NUBPL
0.923 0.036 14 31787845 missense variant A/C,G snp 2.8E-05 6.4E-05 2
rs104894705
NDUFS7
0.846 0.107 19 1391006 missense variant G/A snp 5.6E-05 6.4E-05 2
rs118203929
NDUFAF5
0.923 0.036 20 13801652 missense variant T/C snp 2.0E-05 2
rs104894884
RNF113A ; NDUFA1
0.821 0.107 X 119871933 missense variant G/C snp 2