Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs3775291
TLR3
0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs4848306 0.851 0.120 2 112840530 non coding transcript exon variant G/A snv 0.39 6
rs1799972
OPRM1
0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs9825563
DRD3
1.000 0.080 3 114181373 intron variant A/G snv 0.36 2
rs4704846
HAVCR2
1.000 5 157086333 3 prime UTR variant G/A snv 0.79 2
rs737866
TXNRD2 ; COMT
1.000 0.080 22 19942586 intron variant T/A;C snv 2
rs29221
GABBR1
6 29621347 intron variant C/G snv 0.23 1
rs6902403
IPCEF1 ; OPRM1
6 154157868 3 prime UTR variant T/C snv 0.59 1