Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28935197 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs104894845 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 8
rs104894851 0.925 0.200 X 101398920 stop gained G/T snv 3
rs104894852 0.925 0.200 X 101397871 missense variant T/C snv 3
rs199473684 0.925 0.160 X 101399747 3 prime UTR variant C/T snv 3
rs28935485 0.925 0.160 X 101398534 missense variant G/C snv 3
rs104894846 0.925 0.160 X 101398481 missense variant C/T snv 2
rs727504348 0.925 0.160 X 101397982 missense variant C/T snv 2
rs104894837 1.000 0.160 X 101401743 missense variant G/A snv 1
rs104894839 1.000 0.160 X 101398508 stop gained C/A;T snv 1
rs104894840 1.000 0.160 X 101398906 missense variant C/G;T snv 1
rs104894842 1.000 0.160 X 101398079 stop gained C/T snv 1
rs104894843 1.000 0.160 X 101398075 stop gained G/A;C snv 1
rs104894844 1.000 0.160 X 101397907 stop gained C/A;T snv 5.5E-06 1
rs104894848 1.000 0.160 X 101407710 missense variant C/G snv 1
rs104894849 1.000 0.160 X 101398004 stop gained A/G;T snv 5.5E-06 1
rs1057516429 1.000 0.160 X 101403936 stop gained T/A snv 1
rs1060500747 1.000 0.160 X 101398851 stop gained C/T snv 1
rs111812846 1.000 0.160 X 101398495 missense variant C/G;T snv 1
rs112341092 1.000 0.160 X 101397855 missense variant A/G snv 1
rs1555985200 1.000 0.160 X 101398947 splice acceptor variant C/- del 1
rs1555985827 1.000 0.160 X 101401723 stop gained G/A;T snv 1
rs1555985829 1.000 0.160 X 101401736 missense variant C/A;T snv 1
rs1555985830 1.000 0.160 X 101401740 missense variant C/T snv 1
rs1555987175 1.000 0.160 X 101407831 frameshift variant -/ACGAGGGCCAGGAA delins 1