Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs281860639
MIR6894 ; KDM5C
1.000 0.080 X 53199048 stop gained G/T snv 2
rs370667926
MED23
1.000 6 131603129 missense variant C/T snv 1.6E-05 1.4E-05 2
rs3758653
DRD4
1.000 0.200 11 636399 upstream gene variant T/C snv 0.20 2
rs376285784
TSC2
1.000 0.120 16 2064342 missense variant G/A snv 1.2E-05 2.1E-05 2
rs387906728
UBE2A
1.000 X 119574743 missense variant G/A snv 2
rs61753016
MECP2
1.000 0.200 X 154030614 missense variant G/A snv 6.8E-05 3.9E-05 2
rs6511901
CC2D1A
1.000 0.200 19 13916839 intron variant C/T snv 0.39 2
rs6530893
TUSC3
1.000 0.200 8 15671068 intron variant T/C snv 0.14 2
rs6994908
TUSC3
1.000 0.200 8 15674943 intron variant T/C snv 0.32 2
rs745756308
HNMT ; LOC107985948
1.000 2 138013874 missense variant T/C snv 4.0E-06 2
rs745986648
SGO1-AS1 ; SGO1
1.000 0.200 3 20174431 missense variant C/T snv 1.2E-05 7.0E-06 2
rs747138999
GABRA1
1.000 0.040 5 161895753 missense variant G/T snv 2
rs74900327
SMN2
1.000 0.120 5 70049747 missense variant T/C snv 2
rs749457448
DLG3 ; DLG3-AS1
1.000 0.200 X 70452622 start lost A/G snv 2
rs758252808
HNMT
1.000 2 137970206 missense variant G/A snv 4.1E-06 2
rs768560449
IMMT
1.000 0.160 2 86166521 missense variant A/G snv 8.1E-06 7.0E-06 2
rs770896677
TMTC3
1.000 0.080 12 88153313 missense variant G/A;C snv 1.2E-05; 4.0E-06 2
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 2
rs1554032789
NIPBL
0.925 0.160 5 37048547 missense variant T/A snv 13
rs118203933
CA2
0.925 0.360 8 85473779 missense variant C/T snv 8.0E-06 6
rs886041761
KCNA2
0.925 0.200 1 110603902 missense variant C/T snv 6
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs165656
COMT
0.925 0.200 22 19961340 intron variant G/A;C;T snv 5
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs1404008939
ABCB1
0.925 0.200 7 87504324 missense variant A/C;G snv 4.0E-06 4