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
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs2230912
P2RX7 ; LOC105370032
0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs956572
BCL2
0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs2391191
DAOA-AS1 ; DAOA
0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs5326
DRD1
0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs3916967
DAOA-AS1 ; DAOA
0.882 0.040 13 105464999 intron variant T/C snv 0.32 3
rs6305
HTR2A
0.882 0.040 13 46892487 synonymous variant G/A snv 1.8E-02 1.7E-02 3
rs1046943
MICAL1 ; ZBTB24
1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 3
rs17026688
GADL1
1.000 0.040 3 30845325 intron variant C/T snv 9.3E-03 2
rs781140785
KCNH2
0.925 0.040 7 150952801 missense variant C/T snv 1.2E-05 4.2E-05 2
rs78247304
KCNH7
0.925 0.040 2 162446391 missense variant C/T snv 7.6E-05 6.4E-04 2