Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs1553621496
UNC80
0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs1801260
CLOCK ; TMEM165
0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs28933385
PRNP
0.695 0.320 20 4699818 missense variant G/A snv 4.0E-06 25
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs765798193
PSMD9
0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs5751876
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
0.742 0.320 22 24441333 synonymous variant T/C snv 0.54 0.52 16
rs74315408
PRNP
0.752 0.280 20 4699758 missense variant G/A snv 6.4E-05 4.2E-05 16
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3825172
PSMD9
0.776 0.360 12 121902569 non coding transcript exon variant C/G;T snv 14
rs74421874
PSMD9
0.776 0.360 12 121902546 non coding transcript exon variant G/A snv 0.24 14
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs2298383
ADORA2A-AS1 ; ADORA2A ; SPECC1L-ADORA2A
0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 11
rs1172486173
MIR6890 ; QARS1
0.882 0.160 3 49099606 missense variant T/C snv 4.0E-06 11
rs185476065
MIR6890 ; QARS1
0.882 0.160 3 49100222 missense variant G/A;C;T snv 8.0E-05; 4.0E-06 11
rs74315403
PRNP
0.790 0.200 20 4699752 missense variant G/A snv 10
rs7602358
KLHL30
0.827 0.080 2 238147187 intron variant G/T snv 0.83 6
rs4822492
ADORA2A-AS1
1.000 0.040 22 24447626 intron variant C/G snv 0.47 4
rs76481776
MIR182 ; LOC105375501
0.925 0.200 7 129770387 non coding transcript exon variant C/G;T snv 5.9E-02 4
rs6985606
OPRK1
0.882 0.080 8 53248556 intron variant T/C snv 0.63 4