Disease: Bipolar Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 16
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs33388
NR3C1
0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs779867
GRM7
0.776 0.120 3 7442784 intron variant T/C;G snv 9
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 8
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs12576775
TENM4
0.827 0.080 11 79366149 intron variant A/G snv 0.15 6