Disease: Attention deficit hyperactivity disorder
Source: INFERRED ×
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 15
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
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
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
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
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 5
rs3001723
PTPRF
0.925 0.040 1 43572014 intron variant G/A snv 0.40 2
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 5
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6