Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876657421
CBS
0.763 0.240 21 43063074 coding sequence variant -/CCCAGCAAAAGCCCCACCTGGATGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG;CCCAGCAAAAGCCCCACCTGGGTGATCCACCCCAGTGATCTGCAGAGGGCGCGGCTTCAGGGCTCAAG delins 11
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs9370822
DTNBP1 ; LOC105374947
0.882 0.120 6 15544505 intron variant A/C snv 0.36 7
rs17536211
GABRG1
1.000 0.040 4 46085716 intron variant A/C snv 0.14 3
rs2463107 1.000 0.040 12 79699537 intron variant A/C snv 0.36 2
rs1458103 11 81336231 intron variant A/C snv 0.25 1
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs8192506
DBI
1.000 0.040 2 119372265 missense variant A/C;G snv 4.0E-06; 2.5E-02 2
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs112146896
EFHD2
1.000 0.040 1 15418527 intron variant A/C;G;T snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1390938
SLC18A1
0.807 0.200 8 20179202 missense variant A/G snv 0.71 0.78 7
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6