Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28986206 1.000 0.040 6 32587634 intron variant -/AT ins 1
rs17191234 1.000 0.040 6 32596904 intergenic variant A/C snv 0.34 1
rs28366267 1.000 0.040 6 32592004 upstream gene variant A/C snv 0.25 1
rs28366334 1.000 0.040 6 32594118 upstream gene variant A/C snv 0.26 1
rs481245 1.000 0.040 6 32608337 intergenic variant A/C snv 0.41 1
rs9270593 1.000 0.040 6 32593668 upstream gene variant A/C;G;T snv 1
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs144453041 1.000 0.040 6 32605248 intergenic variant A/G snv 1
rs28366270 1.000 0.040 6 32592157 upstream gene variant A/G snv 0.26 1
rs28366314 1.000 0.040 6 32593424 upstream gene variant A/G snv 0.26 1
rs28366323 1.000 0.040 6 32593832 upstream gene variant A/G snv 0.26 1
rs28366328 1.000 0.040 6 32593989 upstream gene variant A/G snv 0.26 1
rs28366335 1.000 0.040 6 32594134 upstream gene variant A/G snv 0.25 1
rs28366353 1.000 0.040 6 32597227 intergenic variant A/G snv 0.34 1
rs35445101 0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 1
rs614437 1.000 0.040 6 32606164 intergenic variant A/G snv 0.42 1
rs615698 1.000 0.040 6 32606413 intergenic variant A/G snv 0.41 1
rs680151 1.000 0.040 6 32603389 intergenic variant A/G snv 0.41 1
rs9270570 1.000 0.040 6 32593201 upstream gene variant A/G snv 0.51 1
rs9270583 1.000 0.040 6 32593452 upstream gene variant A/G snv 0.48 1
rs9270773 1.000 0.040 6 32601213 intergenic variant A/G snv 0.40 1
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 1
rs9270655 1.000 0.040 6 32598189 intergenic variant A/G;T snv 0.40 1
rs643889 1.000 0.040 6 32608141 intergenic variant A/T snv 0.33 1
rs9270520 1.000 0.040 6 32591716 upstream gene variant A/T snv 0.42 1