Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10503253
CSMD1
0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10744560
CACNA1C ; CACNA1C-IT3
0.882 0.040 12 2277933 intron variant C/G;T snv 3
rs10748045
GRIP1
0.925 0.040 12 66422359 intron variant A/G snv 0.41 3
rs10774035
CACNA1C
0.925 0.040 12 2259508 intron variant C/A;T snv 2
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 3
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
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs10994338
ANK3
0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 3
rs10994359
ANK3
0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs10994397
ANK3
0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11004733
PCDH15
0.882 0.040 10 55089584 intron variant C/T snv 2.9E-02 4
rs11152369
TCF4
0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs11714565
PBRM1 ; SMIM4
0.925 0.040 3 52572276 intron variant C/T snv 0.42 2
rs11720243
PBRM1
0.925 0.040 3 52584002 intron variant T/C snv 0.46 2
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
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
rs12487591
PBRM1
0.925 0.040 3 52608920 intron variant A/T snv 0.34 2
rs12497998
NEK4
0.925 0.040 3 52759586 intron variant C/T snv 0.46 2