Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs863225045
ALDH18A1
0.790 0.360 10 95637327 missense variant C/A;T snv 15
rs875989803
DDX3X
0.827 0.200 X 41343249 stop gained G/T snv 15
rs1559759089
ATP6V1A
0.827 0.200 3 113795101 missense variant C/A snv 14
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 14
rs80338701
PMM2
0.776 0.360 16 8811088 stop gained C/A;T snv 4.4E-05; 5.4E-06 14
rs869312824
GNB1
0.827 0.200 1 1804565 missense variant A/G snv 14
rs138632121
THOC6 ; HCFC1R1
0.776 0.400 16 3026140 missense variant T/A snv 1.7E-04 2.0E-04 13
rs139751598
PYCR1
0.851 0.240 17 81934931 missense variant C/T snv 2.4E-05 4.2E-05 13
rs1555740650
PRR12
0.807 0.240 19 49596253 stop gained G/T snv 13
rs200426926
THOC6 ; BICDL2
0.776 0.400 16 3027379 missense variant G/A;T snv 1.8E-04; 4.0E-06 13
rs672601370
KIF1A
0.790 0.160 2 240775863 missense variant G/A snv 13
rs886039814
WDR19
0.807 0.200 4 39218060 missense variant C/G snv 13
rs886041116
ADNP
0.776 0.240 20 50892526 stop gained G/A snv 13
rs913477149
RFT1
0.851 0.160 3 53105728 missense variant T/A;C snv 13
rs1554386687
CAMK2B
0.882 0.040 7 44242328 missense variant C/T snv 12
rs926027867
CAMK2A
0.882 0.040 5 150251808 missense variant G/A;T snv 12
rs1057520918
CACNA1A
0.790 0.160 19 13262780 missense variant C/T snv 11
rs1135402761
SYT1
0.827 0.320 12 79448958 missense variant T/C snv 11
rs147484110
CSTB
0.807 0.200 21 43774760 splice acceptor variant C/G snv 1.5E-04 2.7E-04 11
rs1567010427
DYNC1H1
0.882 14 102010824 missense variant G/A snv 11
rs188675529
CENPT ; THAP11
0.827 0.240 16 67842794 missense variant C/G;T snv 1.6E-03 6.0E-04 11
rs869312685
ITPR1
0.807 0.240 3 4815135 missense variant G/A;C snv 11
rs869312825
GNB1
0.827 0.120 1 1804548 start lost T/C snv 11
rs886039807
TMEM231
0.776 0.480 16 75541466 non coding transcript exon variant A/G snv 4.2E-06 11
rs121908119
WNT10A ; LOC107984111
0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10