Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3750625
ADRA2A
10 111079843 3 prime UTR variant C/A snv 8.7E-02 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs12654778
ADRB2
5 148826178 5 prime UTR variant G/A snv 0.34 1
rs28362731
AQP1
7 30922175 missense variant G/A snv 3.1E-02 2.6E-02 2
rs887200
ARVCF
22 19976143 intron variant C/T snv 0.74 1
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs179971
ATXN1
6 16362511 intron variant C/T snv 0.66 1
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs893924483
BDNF ; BDNF-AS
0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs1050565
BLMH
1.000 0.080 17 30249058 missense variant T/C snv 0.30 0.29 2
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs3845446
CACNA1E
1 181797301 intron variant T/C snv 6.3E-02 3
rs1044396
CHRNA4
0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1044397
CHRNA4
0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs806378
CNR1
1.000 0.040 6 88149832 intron variant C/T snv 0.21 2
rs1676486
COL11A1
0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 7
rs16868943
COL11A2
1.000 0.040 6 33179950 intron variant G/A snv 2.9E-02 3
rs1554781700
COL5A1
0.851 0.240 9 134701287 missense variant G/T snv 12
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19