Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs397514679
SYN1
0.790 0.200 X 47574321 stop gained G/A snv 9
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
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs6551665
ADGRL3
0.882 0.040 4 61873823 intron variant G/A snv 0.59 4
rs3027407
MAOA
0.925 0.040 X 43745594 3 prime UTR variant A/G snv 3
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50 3
rs587777457
MAOA
0.925 0.200 X 43731695 missense variant G/T snv 3
rs768913131
NRXN1
0.925 0.040 2 50552821 missense variant G/A snv 3
rs10230087
FOXP2
1.000 0.040 7 114614352 intron variant G/A snv 0.73 2
rs1163276899
CACNA1D
1.000 0.040 3 53673125 missense variant G/A snv 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
rs1801291
MAOA
1.000 0.040 X 43744144 synonymous variant T/C snv 2
rs1804197
APC
1.000 0.040 5 112844212 3 prime UTR variant C/A snv 7.2E-02 2
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs2061183
FOXP2
1.000 0.040 7 114617959 intron variant C/G snv 0.73 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614