Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1491942 1.000 0.040 12 40227006 intron variant C/G snv 0.23 1
rs28903073 1.000 0.040 12 40259708 intron variant G/A snv 2.4E-03 1
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 1
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 1
rs76904798 0.925 0.080 12 40220632 intron variant C/T snv 0.13 1