Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35445101 0.925 0.080 6 32579102 missense variant A/G snv 4.2E-04 2.7E-02 1
rs9269749 1.000 0.040 6 32580359 intron variant T/A;C;G snv 1
rs9269761 1.000 0.040 6 32580503 intron variant G/A;C snv 1
rs34309628 1.000 0.040 6 32581554 splice region variant C/A;T snv 0.14; 3.3E-03 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
rs28724033 1.000 0.040 6 32583128 intron variant C/A;T snv 1
rs113520250 1.000 0.040 6 32587108 intron variant C/T snv 0.26 1
rs28986206 1.000 0.040 6 32587634 intron variant -/AT ins 1
rs9270157 1.000 0.040 6 32587634 intron variant C/T snv 0.14 1
rs77122291 1.000 0.040 6 32591242 upstream gene variant G/A snv 0.23 1
rs9270504 1.000 0.040 6 32591407 upstream gene variant C/A snv 0.48 1
rs9270520 1.000 0.040 6 32591716 upstream gene variant A/T snv 0.42 1
rs28366267 1.000 0.040 6 32592004 upstream gene variant A/C snv 0.25 1
rs28366270 1.000 0.040 6 32592157 upstream gene variant A/G snv 0.26 1
rs28366288 1.000 0.040 6 32592655 upstream gene variant C/T snv 0.26 1
rs9270556 1.000 0.040 6 32592829 upstream gene variant G/A snv 0.48 1
rs9270558 1.000 0.040 6 32592890 upstream gene variant G/A snv 0.48 1
rs9270559 1.000 0.040 6 32592921 upstream gene variant T/G snv 0.50 1
rs28366296 1.000 0.040 6 32592950 upstream gene variant C/A snv 0.26 1
rs9270567 1.000 0.040 6 32593024 upstream gene variant T/G snv 0.48 1
rs28366297 1.000 0.040 6 32593052 upstream gene variant G/C snv 0.26 1
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs28366301 1.000 0.040 6 32593106 upstream gene variant G/A snv 0.26 1
rs28366302 1.000 0.040 6 32593157 upstream gene variant G/C snv 0.26 1