Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 13
rs279858
GABRA2
0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs684513
CHRNA5
0.925 0.080 15 78566058 intron variant C/G;T snv 5
rs1455858
LOC349160 ; CHRM2
0.925 0.080 7 136946956 intron variant T/C snv 0.69 3
rs139994842
NOTCH1
0.925 0.040 9 136508308 missense variant G/A;C snv 1.5E-03 3
rs11174811
AVPR1A
1.000 12 63146696 3 prime UTR variant C/A snv 0.12 2
rs3778150
OPRM1
0.925 0.080 6 154062523 intron variant T/C snv 0.17 2
rs3811995
GABRA6
1.000 5 161685687 intron variant C/T snv 0.48 1
rs36021
SLC6A2
1.000 16 55678038 intron variant T/A snv 0.60 1