Disease: Bipolar Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs16976358
LINC00907
0.827 0.080 18 42611606 intron variant T/C snv 1.0E-02 6
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1460808228
PRKCB
0.851 0.040 16 24185518 missense variant T/C snv 7.0E-06 4
rs4446909
ASMT
0.925 0.040 Y 1614890 upstream gene variant G/A snv 2