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
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
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
rs1135402760
BRSK2
0.851 0.160 11 1451405 frameshift variant AG/- delins 6
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909323
CACNA1A
0.790 0.160 19 13277122 stop gained G/A snv 8
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs1554210073
PHIP
0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs1555453538
POLG ; MIR6766
0.807 0.280 15 89326678 frameshift variant A/- delins 7
rs1555565492
RAI1
0.776 0.160 17 17795417 frameshift variant -/G delins 18
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs1562114190
IRAK1BP1 ; PHIP
0.790 0.160 6 78946061 frameshift variant A/- delins 21
rs1562134961
IRAK1BP1 ; PHIP
0.776 0.320 6 78969879 frameshift variant A/- delins 13
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs3746544
SNAP25 ; SNAP25-AS1
0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25