Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28366313 1.000 0.040 6 32593409 upstream gene variant G/A snv 0.26 1
rs28366314 1.000 0.040 6 32593424 upstream gene variant A/G snv 0.26 1
rs28366315 1.000 0.040 6 32593430 upstream gene variant C/T snv 0.26 1
rs28366316 1.000 0.040 6 32593469 upstream gene variant T/C snv 0.26 1
rs28366317 1.000 0.040 6 32593634 upstream gene variant C/T snv 0.26 1
rs28366319 1.000 0.040 6 32593718 upstream gene variant G/A;T snv 1
rs28366320 1.000 0.040 6 32593774 upstream gene variant G/A snv 0.38 1
rs28366323 1.000 0.040 6 32593832 upstream gene variant A/G snv 0.26 1
rs28366327 1.000 0.040 6 32593901 upstream gene variant G/A snv 0.26 1
rs28366328 1.000 0.040 6 32593989 upstream gene variant A/G snv 0.26 1
rs28366330 1.000 0.040 6 32594069 upstream gene variant G/C;T snv 1
rs28366331 1.000 0.040 6 32594103 upstream gene variant T/G snv 0.26 1
rs28366334 1.000 0.040 6 32594118 upstream gene variant A/C snv 0.26 1
rs28366335 1.000 0.040 6 32594134 upstream gene variant A/G snv 0.25 1
rs28366341 1.000 0.040 6 32597007 intergenic variant G/C snv 0.34 1
rs28366344 1.000 0.040 6 32597036 intergenic variant T/C snv 0.34 1
rs28366351 1.000 0.040 6 32597213 intergenic variant G/A snv 0.34 1
rs28366352 1.000 0.040 6 32597216 intergenic variant T/C snv 0.34 1
rs28366353 1.000 0.040 6 32597227 intergenic variant A/G snv 0.34 1
rs28366356 1.000 0.040 6 32597314 intergenic variant G/T snv 0.34 1
rs28366357 1.000 0.040 6 32597361 intergenic variant C/T snv 0.34 1
rs28366362 1.000 0.040 6 32597436 intergenic variant T/A;C snv 1
rs2858866 1.000 0.040 6 32607614 intergenic variant G/C;T snv 1
rs28724008 1.000 0.040 6 32582773 intron variant C/G snv 0.14 1
rs28724031 1.000 0.040 6 32583042 intron variant C/A snv 0.27 1