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
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
rs56149945
NR3C1
0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs6323
MAOA
0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs10492664 0.925 0.040 13 108163877 intergenic variant C/A;T snv 2
rs9291283
GABRA2
0.925 0.080 4 46369816 intron variant G/A;T snv 2
rs13398848 1.000 0.040 2 84018044 intergenic variant A/G snv 7.5E-02 1
rs16831128 1.000 0.040 2 132386819 intergenic variant A/G snv 0.19 1
rs7950811 1.000 0.040 11 92917836 intron variant C/A;T snv 1
rs383902
ADAM10
1.000 0.040 15 58741975 intron variant C/T snv 0.49 1
rs16891867
C1QTNF7-AS1 ; C1QTNF7
1.000 0.040 4 15395740 intron variant A/G snv 0.11 1
rs1861046
C1QTNF7 ; C1QTNF7-AS1
1.000 0.040 4 15396282 intron variant G/A snv 0.11 1
rs2053053
CAMK2A
1.000 0.040 5 150229830 intron variant G/A;C snv 1
rs11838918
LINC00331
1.000 0.040 13 78836439 intron variant T/C snv 2.3E-02 1
rs7762160
PDE10A
1.000 0.040 6 165601943 intron variant T/C snv 0.36 1