Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008723 0.925 0.160 17 39910014 intron variant G/C;T snv 3
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
rs12936231 0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs17498196 1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 2
rs2066362 1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs3771166 1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs3771180 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795405 0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 3
rs869402 0.925 0.160 17 39911790 intron variant T/A;C snv 3
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 2
rs9303280 1.000 0.080 17 39917778 non coding transcript exon variant T/A;C snv 2
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2