Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs74315457
ARSA
0.851 0.160 22 50626976 missense variant A/C snv 2.3E-04 2.8E-04 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs806371
CNR1
0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs1198588 1.000 0.040 1 98087276 intergenic variant A/T snv 0.78 2
rs2455391
SLC6A3
1.000 0.040 5 1443383 intron variant G/A snv 0.20 2
rs7549184 1 215239563 downstream gene variant G/A;C snv 1
rs10779646
KCNK2
1 215152892 intron variant G/A snv 0.56 1