Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs10744560
CACNA1C ; CACNA1C-IT3
0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs10774035
CACNA1C
0.925 0.040 12 2259508 intron variant C/A;T snv 2
rs10835210
BDNF ; BDNF-AS
0.882 0.040 11 27674363 intron variant C/A;G snv 4
rs10865974
PBRM1 ; GNL3
0.925 0.040 3 52684264 intron variant G/C;T snv 2
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12487445
PBRM1
0.925 0.040 3 52584303 intron variant A/C;T snv 2
rs12635140
SPCS1 ; GLT8D1
0.925 0.040 3 52704149 intron variant T/A;C snv 2
rs12649507
CLOCK
0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs13068293
PBRM1
0.925 0.040 3 52638151 intron variant C/A;G snv 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17211233
RASGRF2
0.882 0.040 5 81072944 intron variant T/A;C snv 4
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2075984
TPTEP2-CSNK1E ; CSNK1E
0.882 0.040 22 38294883 intron variant C/A;G;T snv 3
rs2336146
PBRM1
0.925 0.040 3 52592630 intron variant A/G;T snv 2
rs2336149
PBRM1
0.925 0.040 3 52658108 intron variant G/A;C snv 2
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs3733045
PBRM1
0.925 0.040 3 52609291 non coding transcript exon variant A/G;T snv 0.44 2
rs3755798
GLT8D1 ; SPCS1
0.925 0.040 3 52707144 non coding transcript exon variant G/A;C snv 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306