Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs864321670
ALDH18A1
0.763 0.320 10 95633012 missense variant C/T snv 24
rs1557055405
ABCD1
0.807 0.400 X 153743532 missense variant T/A snv 21
rs1565930588
HSPB8
0.882 0.160 12 119193787 frameshift variant TACTCAACATTTGG/- del 19
rs4645981
CASP9 ; DNAJC16
0.790 0.160 1 15524988 intron variant G/A;C snv 11
rs4645978
CASP9 ; DNAJC16
0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs1564691414
FAS
0.925 0.160 10 89007698 splice acceptor variant A/G snv 7