Disease: Bipolar Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs2239547
ITIH4
0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs11789399
LOC105376249
0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs4765905
CACNA1C
0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5