Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs539703 0.882 0.200 6 32320685 intron variant A/C;T snv 4
rs926591 0.882 0.200 6 32337913 intron variant C/A snv 0.33 4
rs4959093 0.882 0.200 6 32345320 intron variant T/C snv 0.33 4
rs574710 0.882 0.200 6 32320413 intron variant T/C snv 0.34 4
rs9268402 0.827 0.200 6 32373576 intron variant G/A snv 0.45 4
rs9368716 0.882 0.200 6 32338313 intron variant G/A snv 0.39 4
rs3129900 0.882 0.200 6 32338202 intron variant G/T snv 0.83 3
rs6907322 1.000 0.080 6 32357168 intron variant G/A snv 0.25 2
rs910050 0.925 0.120 6 32347877 intron variant G/C snv 0.42 2
rs9268302 1.000 0.080 6 32357040 intron variant C/T snv 0.29 2
rs544358 0.925 0.120 6 32305381 intron variant G/C snv 0.33 2