Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894681 0.776 0.200 19 46756793 missense variant C/T snv 9.0E-06 10
rs104894682 0.925 0.160 19 46756936 stop lost T/A snv 8.1E-06 1.4E-05 2
rs104894683 1.000 0.120 19 46755685 missense variant G/A snv 1.0E-03 4.3E-03 1
rs104894689 1.000 0.120 19 46756214 stop gained G/A snv 1
rs104894690 1.000 0.120 19 46755850 missense variant C/T snv 1
rs104894691 0.925 0.160 19 46756349 missense variant T/C snv 6.4E-06 4.2E-05 2
rs104894692 0.882 0.160 19 46756369 missense variant T/A snv 6.3E-06 1.4E-05 3
rs1191737604 1.000 0.120 19 46756004 frameshift variant C/-;CC delins 1
rs1301397800 1.000 0.120 19 46756883 missense variant T/C snv 4.1E-06 7.0E-06 1
rs143031195 1.000 0.120 19 46756523 missense variant C/T snv 1.4E-04 1.0E-04 1
rs1450841129 1.000 0.120 19 46756466 missense variant G/A;C;T snv 5.2E-06 1
rs148206382 1.000 0.120 19 46755877 missense variant C/A snv 4.5E-03 3.6E-03 1
rs1483781400 1.000 0.120 19 46756381 stop gained G/A;T snv 1
rs1555735545 0.851 0.160 19 46746071 5 prime UTR variant G/A snv 22
rs1555738149 1.000 0.120 19 46755617 frameshift variant -/AGGCATTTGACAACGCG delins 1
rs1555738201 1.000 0.120 19 46755664 stop gained C/T snv 1
rs1555738204 1.000 0.120 19 46755671 frameshift variant -/AGCCC delins 1
rs1555738245 1.000 0.120 19 46755717 frameshift variant G/AT delins 1
rs1555738311 1.000 0.120 19 46755794 frameshift variant GCGCC/- delins 1
rs1555738456 1.000 0.120 19 46755914 frameshift variant T/- del 1
rs1555738502 1.000 0.120 19 46755976 stop gained C/T snv 1
rs1555738568 1.000 0.120 19 46756012 frameshift variant -/CCCGC delins 1
rs1555738651 1.000 0.120 19 46756104 frameshift variant G/- delins 1
rs1555738675 1.000 0.120 19 46756131 frameshift variant GGCTGGGCGGTGCAGCTGCTGGACTTGACCTTCGC/- delins 1
rs1555738686 1.000 0.120 19 46756136 frameshift variant G/- del 1