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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs80338903
USH2A
0.701 0.360 1 216247095 frameshift variant C/- del 7.6E-04 5.4E-04 25
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs28936375
CPT2
0.752 0.320 1 53197092 missense variant C/A snv 1.7E-04 2.2E-04 15
rs769540300
OPRM1
0.851 0.200 6 154091047 missense variant G/A snv 1.2E-05 8
rs1800866
SIGMAR1
0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 8
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs41292285
CACNA1H
1.000 0.040 16 1208033 missense variant G/T snv 7.3E-03 7.1E-03 3
rs540638287
CACNA1H
1.000 0.040 16 1204313 missense variant C/T snv 4.3E-05 1.4E-05 3
rs3781719
CALCB ; CALCA
1.000 0.040 11 14972978 intron variant A/G snv 0.35 2
rs614230
CX3CL1
1.000 0.040 16 57385374 downstream gene variant C/T snv 0.61 2
rs200207721
OPRM1
6 154039743 missense variant A/G snv 1.2E-05 1.4E-05 2
rs77114424
OPRM1
6 154039497 missense variant G/A snv 2