Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs16836940
RPRD2
0.925 0.040 1 150444437 intron variant A/G snv 0.31 2
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325
BCL9
0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs946903
BCL9
0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs12476147
ZNF804A
0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs149268645
WDR12 ; CARF
0.882 0.040 2 202968295 intron variant G/A snv 8.4E-02 4
rs17662626
LOC107985969
0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5