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
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 25
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs2075786
TERT
0.790 0.360 5 1266195 intron variant A/G snv 0.55 8
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs1860545
TNFRSF1A
0.790 0.200 12 6337611 intron variant G/A snv 0.31 7
rs4149577
TNFRSF1A
0.827 0.280 12 6338356 intron variant G/A;T snv 7
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs2769605 0.827 0.040 9 85297756 intergenic variant C/T snv 0.44 5
rs2736118
TERT
0.882 0.120 5 1260080 intron variant T/C snv 0.33 4
rs562047
HSPA1L ; HSPA1A
0.882 0.080 6 31816086 missense variant G/C snv 0.16 3
rs1387923
NTRK2
0.882 0.040 9 85025721 3 prime UTR variant A/G snv 0.47 3
rs1565445
NTRK2
0.882 0.040 9 85002156 intron variant G/A snv 0.74 3
rs4149576
TNFRSF1A
0.882 0.200 12 6339949 intron variant C/T snv 0.32 3
rs3751082
ALDH3B1
0.925 0.160 11 68027885 synonymous variant G/A snv 0.21 0.19 2
rs983583
YWHAZ
0.925 0.080 8 100949682 intron variant T/C snv 0.66 2
rs117610176
DTNBP1 ; LOC105374947
1.000 0.040 6 15524368 3 prime UTR variant A/G snv 5.6E-03 1.7E-03 1