Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs80338842
TIMM8B ; SDHD
0.790 0.280 11 112086910 start lost G/A;C snv 8
rs1131691061
SDHB
0.827 0.280 1 17054017 start lost C/T snv 6
rs587776652
SDHC
0.882 0.200 1 161314408 start lost G/A snv 4
rs878854590
SDHD
0.851 0.240 11 112088869 frameshift variant G/- delins 4
rs104894033
OPN1SW ; CALU
0.925 0.120 7 128773786 missense variant G/A snv 3.2E-05 3.5E-05 3
rs11203289
SDHB
0.882 0.240 1 17054012 missense variant G/A;C snv 4.1E-06; 3.1E-03 3
rs1398198098
CCDC127 ; SDHA
1.000 0.120 5 218363 missense variant G/C snv 1
rs104894031
OPN1SW
1.000 0.120 7 128775556 missense variant C/T snv 3.3E-04 1.7E-04 1
rs104894032
OPN1SW
1.000 0.120 7 128774545 missense variant A/C;G snv 3.2E-05; 1.2E-05 1
rs1190183515
OPN1SW
1.000 0.120 7 128774616 missense variant G/A snv 1