Disease: Major Depressive Disorder
Source: GWASDB ×
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 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 3
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 2
rs10774037
CACNA1C
0.882 0.040 12 2311360 intron variant G/A snv 0.77 2
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 2
rs10994338
ANK3
0.882 0.040 10 60421370 intron variant G/A snv 7.5E-02 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
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
rs1866268
PBRM1 ; GNL3
0.925 0.040 3 52685382 intron variant C/A snv 0.46 2
rs1938526
ANK3
0.882 0.040 10 60540625 intron variant A/G snv 8.3E-02 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