Disease: Attention deficit hyperactivity disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs130058
HTR1B ; LOC105377864
0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1715
ZNF615
0.851 0.040 19 51991525 3 prime UTR variant T/C snv 1.4E-05 5
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5