Disease: Attention deficit hyperactivity disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs534654
TMEM165
0.925 0.040 4 55424053 non coding transcript exon variant A/G snv 0.81 2
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs13061878
PTPRG
0.925 0.040 3 61634560 intron variant A/T snv 9.7E-02 2
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs11756438
CEP85L
0.925 0.040 6 118672469 intron variant C/A snv 0.42 3
rs12661338
CEP85L ; LOC105377971
0.925 0.040 6 118473527 intron variant C/A snv 0.35 2
rs7089973
TAF9BP2 ; ABLIM1
0.925 0.040 10 114809806 intron variant C/A snv 0.41 2
rs71420669
LOC105376755
0.925 0.040 2 194986941 intergenic variant C/A snv 6.6E-02 2