Disease: Major Depressive Disorder
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008257 0.925 0.040 4 94435177 intergenic variant G/A snv 0.63 2
rs10774035
CACNA1C
0.925 0.040 12 2259508 intron variant C/A;T snv 2
rs10865974
PBRM1 ; GNL3
0.925 0.040 3 52684264 intron variant G/C;T snv 2
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
rs11773103
DMTF1
0.925 0.040 7 87192664 non coding transcript exon variant A/G snv 4.5E-02 2
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
rs12635140
SPCS1 ; GLT8D1
0.925 0.040 3 52704149 intron variant T/A;C snv 2
rs13064064
PBRM1
0.925 0.040 3 52622986 intron variant T/C snv 0.34 2
rs13068293
PBRM1
0.925 0.040 3 52638151 intron variant C/A;G snv 2
rs1561337
PBRM1
0.925 0.040 3 52625947 intron variant G/A snv 0.34 2
rs16836940
RPRD2
0.925 0.040 1 150444437 intron variant A/G snv 0.31 2
rs17082664
SYNE1
0.925 0.040 6 152417619 intron variant A/G snv 0.17 2
rs1866268
PBRM1 ; GNL3
0.925 0.040 3 52685382 intron variant C/A snv 0.46 2
rs1961958
PBRM1 ; SMIM4
0.925 0.040 3 52551974 intron variant A/G snv 0.34 2
rs2072390
NEK4
0.925 0.040 3 52746493 intron variant A/T snv 0.46 2
rs2230535
NEK4
0.925 0.040 3 52766268 synonymous variant T/C snv 0.40 0.34 2
rs2268026
NEK4
0.925 0.040 3 52744331 intron variant T/C snv 0.40 0.34 2
rs2289247
GNL3 ; SNORD69
0.925 0.040 3 52693241 missense variant G/A snv 0.43 0.46 2
rs2289250
PBRM1
0.925 0.040 3 52648930 intron variant C/A snv 0.34 2
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
rs2336545
NEK4
0.925 0.040 3 52753587 non coding transcript exon variant T/C snv 0.34 2