Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893991 0.925 0.120 6 45438040 missense variant G/A snv 2
rs104893993 0.925 0.120 6 45437964 missense variant A/G snv 2
rs104893988 1.000 0.080 6 45512277 stop gained G/A snv 1
rs104893989 1.000 0.080 6 45431963 missense variant T/C;G snv 2.0E-05 1
rs104893990 1.000 0.080 6 45432011 missense variant G/A snv 1
rs104893992 1.000 0.080 6 45438039 missense variant C/T snv 1
rs104893994 1.000 0.080 6 45547304 stop lost G/C snv 1
rs104893995 1.000 0.080 6 45431945 missense variant G/A;C snv 4.0E-06 1
rs1057521068 1.000 0.080 6 45432008 missense variant G/A snv 1
rs1428979499 1.000 0.080 6 45431875 missense variant G/A snv 4.0E-06 1
rs397515537 1.000 0.080 6 45546910 stop gained C/T snv 1
rs397515538 1.000 0.080 6 45422618 frameshift variant C/-;CC delins 1
rs730880313 1.000 0.080 6 45422723 frameshift variant GCAGCAACAGCAGCA/ACAGCAGCAGCAGCAGCAGCAACAGCAGCCG delins 1
rs730880315 1.000 0.080 6 45546964 frameshift variant -/C delins 1
rs752933596 1.000 0.080 6 45438020 missense variant A/T snv 1
rs759100705 1.000 0.080 6 45431872 missense variant C/T snv 8.0E-06 1
rs864621970 1.000 0.080 6 45431915 missense variant G/A snv 1
rs201647225 1.000 0.080 6 45431962 missense variant A/G snv 1.1E-04 6.3E-05 1