Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs3915512
DLG1 ; MIR4797
1.000 0.040 3 197295369 intron variant A/G;T snv 3
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs4680612 1.000 0.040 3 165891643 intergenic variant G/A snv 0.95 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs59190448
OXTR ; CAV3
3 8761315 intron variant G/A snv 0.12 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs148789453
IDUA
0.882 0.120 4 1001802 missense variant T/A;G snv 2.2E-05; 4.4E-06 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs1800044
HTR1A
0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 4
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs1799920
HTR1A
5 63961656 missense variant C/G;T snv 3.2E-04 2
rs1799921
HTR1A
5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169