Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs992670
C5
0.882 0.120 9 121019492 intron variant G/A snv 0.52 3
rs987195
MIR155HG
0.925 0.040 21 25565010 intron variant C/G;T snv 2
rs9833158
LOC105377641
1.000 0.040 3 16742882 intergenic variant G/A snv 0.53 1
rs982953473
SCN2A
1.000 0.040 2 165354456 missense variant G/A snv 2.1E-05 1
rs970510
LOC102725148
1.000 0.040 18 71812685 intergenic variant T/A snv 0.78 2
rs969885 0.925 0.040 21 25558821 upstream gene variant C/T snv 8.2E-02 2
rs9694676
LRP12
0.925 0.080 8 104588948 5 prime UTR variant A/G snv 8.6E-02 0.20 2
rs9596863
LINC00558
1.000 0.040 13 53860512 intron variant T/G snv 0.11 2
rs9596837 1.000 0.040 13 53683928 intron variant T/C snv 0.11 2
rs945564833
SORBS1
1.000 0.040 10 95381740 missense variant T/C snv 1
rs9390754
GRIK2
1.000 0.040 6 101517038 intron variant A/G snv 0.20 1
rs9331949
CLU ; EPHX2
0.925 0.080 8 27597169 3 prime UTR variant T/C snv 6.2E-02 4.7E-02 2
rs9314349
CLU
1.000 0.040 8 27616685 upstream gene variant A/G snv 0.30 1
rs915895
NOTCH4
1.000 0.040 6 32222440 intron variant T/C snv 0.34 1
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs886044717
KCNT1
0.925 0.040 9 135779423 missense variant T/A snv 3
rs886039903
FGF12
0.807 0.200 3 192335434 missense variant C/T snv 6
rs886039798
ZDHHC24 ; BBS1
0.925 0.120 11 66529902 frameshift variant -/T delins 4
rs886039469
KCNMA1-AS1 ; KCNMA1
0.701 0.560 10 76891709 missense variant T/C snv 35
rs886039278
DEPDC5
1.000 0.040 22 31815000 missense variant G/A snv 4.0E-06 1.4E-05 1
rs880626
RORA
1.000 0.040 15 60691230 intron variant G/A snv 0.30 1
rs879255652
SCN8A
0.807 0.120 12 51790425 stop gained G/A;T snv 7
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 4
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs869312865
GRIN1 ; LOC105376328
0.827 0.160 9 137156676 missense variant G/A;C snv 5