Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs3836790
SLC6A3
0.882 0.080 5 1411740 intron variant -/ACATACACACTCAGACACACATACCATGCA ins 5
rs2284411
GRIN2B
1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
rs2161961
GNAL
18 11774501 intron variant A/G snv 0.31 3
rs363043
SNAP25-AS1 ; SNAP25
0.925 0.080 20 10245498 intron variant C/T snv 0.30 3
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2
rs1541665
KCNIP1
1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 2
rs2944366
SLC6A1 ; SLC6A1-AS1
1.000 0.040 3 11011556 intron variant T/C snv 0.25 2
rs402691
PRKCG
19 53888383 intron variant T/C snv 0.39 2
rs9990174
SLC6A1
1.000 0.040 3 10998753 intron variant G/T snv 0.31 2
rs773857
CPAMD8
19 16908042 intron variant C/T snv 0.56 1
rs914655
C9orf92
9 16208133 intron variant G/T snv 1.6E-02 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs945270 0.925 0.040 14 55733755 intergenic variant C/G;T snv 3
rs555145190
NAGLU
0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs387906846
ARID1A
0.807 0.280 1 26773716 stop gained C/G;T snv 19
rs61751362
MECP2
0.790 0.160 X 154030948 stop gained G/A;C snv 1.6E-05 14
rs1057518644
HGSNAT
0.925 0.120 8 43192413 stop gained C/T snv 10
rs1057519475
FOXC1
1.000 0.080 6 1610761 stop gained C/T snv 2
rs372857241
FOXC1
1.000 0.080 6 1610586 stop gained C/G;T snv 1.8E-05 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614