Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555274365 1.000 0.120 13 77000729 frameshift variant GGAA/- delins 1
rs1555274369 1.000 0.120 13 77000796 frameshift variant A/- delins 1
rs1555274373 1.000 0.120 13 77000808 frameshift variant T/- delins 1
rs1555274387 1.000 0.120 13 77000883 frameshift variant T/- delins 1
rs1566219136 1.000 0.120 13 76995993 missense variant G/A snv 1
rs200348035 1.000 0.120 13 76992182 stop gained G/A;T snv 4.5E-06 1
rs267606738 1.000 0.120 13 76995119 missense variant G/A snv 1
rs386833963 1.000 0.120 13 77000771 stop gained C/A snv 1
rs386833964 1.000 0.120 13 77000813 frameshift variant CT/- delins 1
rs386833965 1.000 0.120 13 77000817 frameshift variant TT/- del 1
rs386833968 1.000 0.120 13 77000882 stop gained G/A;T snv 4.3E-06 1
rs386833970 1.000 0.120 13 76992238 frameshift variant -/C delins 1
rs386833971 1.000 0.120 13 76995175 stop gained C/T snv 2.4E-05 1
rs386833972 1.000 0.120 13 76995939 stop gained T/G snv 4.0E-06; 4.0E-06 1
rs386833973 1.000 0.120 13 76995942 frameshift variant -/A ins 1
rs386833974 1.000 0.120 13 76995980 stop gained C/T snv 1
rs386833976 1.000 0.120 13 76996008 missense variant T/C snv 4.0E-06 1
rs386833977 1.000 0.120 13 76996028 missense variant C/T snv 1
rs386833978 1.000 0.120 13 76996035 missense variant G/C snv 1
rs386833982 1.000 0.120 13 77000663 frameshift variant A/- delins 1
rs386833983 1.000 0.120 13 77000695 frameshift variant GGAAATGAAACATCTG/- delins 1
rs730882146 1.000 0.120 13 77000680 missense variant G/A snv 4.0E-06 1
rs750935331 1.000 0.120 13 77000850 stop gained C/G;T snv 4.1E-06 1
rs764495616 1.000 0.120 13 77000685 stop gained G/C;T snv 1
rs780198002 1.000 0.120 13 76992229 frameshift variant TC/- delins 9.5E-06 1