Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554887097
MRPL43 ; TWNK
0.807 0.320 10 100989331 missense variant G/A snv 10
rs113994099
POLG
0.827 0.240 15 89320883 missense variant T/C snv 10
rs758026634
MRPL43 ; TWNK
0.827 0.240 10 100989280 missense variant G/A;C snv 2.0E-05 5
rs104894632
MILR1 ; POLG2
0.925 0.200 17 64477929 missense variant C/T snv 2
rs121918055
POLG ; MIR6766
0.925 0.200 15 89326965 missense variant C/T snv 2
rs28999114
SLC25A4
0.925 0.200 4 185144963 missense variant A/G snv 2
rs1057521899
TK2
1.000 0.200 16 66512039 missense variant T/A;G snv 2
rs1085307937
TWNK
0.925 0.200 10 100989835 missense variant G/A snv 2
rs1380006580
CPOX
1.000 0.200 3 98591126 missense variant C/T snv 1
rs17850455
MILR1 ; POLG2
1.000 0.200 17 64480334 missense variant C/G snv 1.0E-02 1.0E-02 1
rs1408088932
MRPL43 ; TWNK
1.000 0.200 10 100988626 missense variant G/A snv 7.0E-06 1
rs1463467386
POLG ; MIR6766
1.000 0.200 15 89327059 missense variant T/C;G snv 4.0E-06 1.4E-05 1
rs762436636
TWNK
1.000 0.200 10 100993419 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 1