Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs1414334
HTR2C
0.851 0.160 X 114903581 intron variant C/G snv 5
rs2279357
CYP11A1
0.851 0.160 15 74338282 intron variant T/C snv 0.69 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs6551665
ADGRL3
0.882 0.040 4 61873823 intron variant G/A snv 0.59 4
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs10230087
FOXP2
1.000 0.040 7 114614352 intron variant G/A snv 0.73 2
rs12531289
FOXP2
1.000 0.040 7 114600061 intron variant T/A snv 0.73 2
rs1350135
FOXP2
1.000 0.040 7 114602621 intron variant C/A;G;T snv 2
rs2061183
FOXP2
1.000 0.040 7 114617959 intron variant C/G snv 0.73 2
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs121918799
SCN1A-AS1 ; SCN1A ; LOC102724058
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs141441277
SYTL4
0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 5
rs779545541
GPHN
0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5