Disease: Bipolar Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3733041
GLT8D1
0.925 0.040 3 52697582 intron variant T/C snv 0.46 2
rs3733045
PBRM1
0.925 0.040 3 52609291 non coding transcript exon variant A/G;T snv 0.44 2
rs3755798
GLT8D1 ; SPCS1
0.925 0.040 3 52707144 non coding transcript exon variant G/A;C snv 2
rs3755806
PBRM1
0.925 0.040 3 52609669 synonymous variant T/C snv 0.39 0.34 2
rs3774366
PBRM1
0.925 0.040 3 52607239 intron variant T/C snv 0.46 2
rs3796353
SMIM4 ; PBRM1
0.925 0.040 3 52559214 intron variant C/T snv 0.42 2
rs4765914
CACNA1C
0.925 0.040 12 2311211 intron variant T/C;G snv 2
rs6762813
GNL3 ; SNORD69
0.925 0.040 3 52692679 intron variant C/T snv 0.33 2
rs6778844
PBRM1 ; SMIM4
0.925 0.040 3 52562382 intron variant T/C snv 0.33 2
rs6804145
PBRM1
0.925 0.040 3 52660182 intron variant C/T snv 0.46 2
rs7297582
CACNA1C
0.925 0.040 12 2246640 intron variant C/T snv 0.29 2
rs7611731
PBRM1
0.925 0.040 3 52658705 intron variant T/C snv 0.46 2
rs7652191
SMIM4 ; PBRM1
0.925 0.040 3 52576399 intron variant T/C snv 0.46 2
rs10744560
CACNA1C ; CACNA1C-IT3
0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs10748045
GRIP1
0.925 0.040 12 66422359 intron variant A/G snv 0.41 3
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
rs10994338
ANK3
0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs140504
LOC107985554 ; BCR
0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs17387100
PROM1
0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 3
rs1938526
ANK3
0.882 0.040 10 60540625 intron variant A/G snv 8.3E-02 3
rs2075984
TPTEP2-CSNK1E ; CSNK1E
0.882 0.040 22 38294883 intron variant C/A;G;T snv 3