Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10947563
FKBP5
0.925 0.040 6 35685660 intron variant G/A snv 0.77 3
rs12701020
CRHR2
0.925 0.040 7 30655345 intron variant C/T snv 0.12 3
rs3798347
FKBP5 ; LOC112267956
0.925 0.040 6 35633999 intron variant A/T snv 0.65 3
rs10083466
NRXN3
1.000 0.040 14 79518375 intron variant C/A snv 0.39 1
rs113507694
DPPA3
1.000 0.040 12 7714013 intron variant A/G snv 3.2E-02 1
rs4713902
LOC112267956 ; FKBP5
1.000 0.040 6 35646249 intron variant T/C snv 0.21 1
rs9470079
FKBP5
1.000 0.040 6 35675286 intron variant G/A snv 0.19 1
rs4722999
CRHR2
0.851 0.080 7 30654159 intron variant C/T snv 0.67 5
rs12718541
FIGNL1 ; DDC
0.925 0.080 7 50482446 intron variant A/G snv 0.55 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs28364997
SLC6A3
0.807 0.120 5 1403013 missense variant G/A snv 5.3E-04 5.8E-04 9
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 8
rs1386494
TPH2
0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs2279709
SLC18A1
0.882 0.120 8 20178722 intron variant T/G snv 0.51 5
rs61749465
MCPH1
0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs2709370 0.851 0.120 2 207517878 intron variant A/C snv 0.17 4
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4
rs6785
CREB1 ; METTL21A
0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs12290811
TENM4
0.882 0.120 11 79372576 intron variant T/A snv 0.18 3
rs175174
ZDHHC8
0.882 0.120 22 20140031 non coding transcript exon variant A/G snv 0.44 3
rs2270637
SLC18A1
0.882 0.120 8 20179316 missense variant C/G snv 0.20 0.21 3
rs2270641
SLC18A1
0.882 0.120 8 20180955 missense variant T/C;G snv 0.32 3