Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3827735
TRIM33
1.000 0.040 1 114510087 intron variant C/A;T snv 1
rs4366301
TSNAX-DISC1 ; DISC1
1.000 0.040 1 231670540 intron variant G/A;C snv 1
rs4925506 1.000 0.040 1 229676242 intergenic variant C/G;T snv 1
rs6537825
TRIM33
1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs6537835 1.000 0.040 1 114566293 downstream gene variant G/A snv 0.80 1
rs6661053
TRIM33
1.000 0.040 1 114496497 intron variant T/A;C snv 1
rs6668845
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231872801 intron variant A/G snv 0.12 1
rs7511633
TRIM33
1.000 0.040 1 114456655 intron variant G/A snv 0.36 1
rs759392137
RIMS3
1.000 0.040 1 40626666 missense variant T/C;G snv 1.6E-05 1
rs841361
LOC105378860 ; SLC44A3-AS1
1.000 0.040 1 94686257 intron variant C/T snv 0.48 1
rs8453
CSDE1 ; NRAS
1.000 0.040 1 114716978 3 prime UTR variant G/T snv 0.11 1
rs926938
AMPD1
1.000 0.040 1 114697195 upstream gene variant A/G;T snv 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1558373252
LINC01248 ; SOX11
0.790 0.120 2 5693013 frameshift variant T/- delins 19
rs794726827
SCN1A ; SCN1A-AS1
0.827 0.120 2 166054637 splice donor variant C/A;G;T snv 6
rs1057521223
SCN2A
1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs2056202
SLC25A12
0.882 0.040 2 171855970 intron variant T/C snv 0.81 0.77 4
rs2292813
SLC25A12
0.882 0.040 2 171787719 intron variant T/C snv 0.81 3
rs768407867
CHRNA1
0.925 0.160 2 174748177 missense variant C/T snv 4.4E-05 3.5E-05 3
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs2018650
LOC100132215 ; EHBP1
0.925 0.040 2 63045589 3 prime UTR variant T/C snv 0.11 2
rs6735330
XPO1
0.925 0.040 2 61504343 intron variant G/A snv 0.18 2
rs7603001
ZNF804A
0.925 0.040 2 184902089 intron variant A/G;T snv 2
rs7608798
DPP4
0.925 0.040 2 162033707 intron variant G/A snv 0.35 2