Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs68081839
GRIA4
0.882 0.080 11 105762027 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTTTTTT delins 3
rs201203751
FYB1
0.925 0.040 5 39203496 intron variant TT/-;T;TTT delins 3
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs1488864
LOC101927825 ; CAVIN3
0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs1535255
CNR1
0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4512342
NRG1
0.827 0.120 8 32750356 intron variant T/G snv 0.12 5
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs806371
CNR1
0.882 0.040 6 88146644 intron variant T/G snv 0.18 4
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs1137070
MAOA
0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs11989919
NRG1
0.882 0.040 8 32645107 intron variant T/C snv 0.10 3
rs12720071
CNR1
0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs1352618632
STARD13
0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs16935279
LINC01592
0.851 0.040 8 68961217 intron variant T/C snv 1.9E-02 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3