Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2073643 1.000 0.080 5 132387596 intron variant T/C snv 0.46 4
rs1158867 1.000 0.080 2 127419801 splice region variant C/T snv 0.51 3
rs3859192 0.925 0.080 17 39972395 intron variant C/T snv 0.42 3
rs4795400 0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs907092 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 3
rs10056340 0.925 0.080 5 110854353 intergenic variant T/G snv 0.31 2
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10206753 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs1043828 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs11078927 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs12734001 1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05 2
rs13408569 1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661 1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 2
rs17498196 1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs2066362 1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs3771166 1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs3771175 0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 2