Disease: Bipolar Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs3788533
PLA2G6
0.925 0.040 22 38127239 non coding transcript exon variant C/G snv 0.47 3
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs778294
DAOA ; DAOA-AS1
0.851 0.040 13 105489886 synonymous variant C/A;T snv 0.27; 4.0E-06 0.26 5
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9