Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908668 0.882 0.240 11 68357673 missense variant G/T snv 5
rs121908674 0.882 0.160 11 68410076 missense variant C/G;T snv 3
rs80358305 0.882 0.160 11 68348188 missense variant C/T snv 3
rs80358313 0.882 0.160 11 68406550 missense variant G/A;C;T snv 1.2E-05; 1.2E-05; 3.2E-05 3
rs1320065036 0.925 0.160 11 68386342 missense variant C/T snv 4.0E-06 7.0E-06 2
rs1057519574 1.000 0.120 11 68347960 missense variant G/T snv 1
rs1057519575 1.000 0.120 11 68446434 splice acceptor variant A/G snv 1
rs1158745675 1.000 0.120 11 68386367 stop gained C/A;T snv 4.0E-06; 4.0E-06 1
rs121908660 1.000 0.120 11 68312743 stop gained G/A snv 1
rs121908661 1.000 0.120 11 68386582 stop gained C/T snv 1
rs121908662 1.000 0.120 11 68409971 frameshift variant -/T delins 1
rs121908663 1.000 0.120 11 68413742 stop gained C/T snv 1
rs121908664 1.000 0.120 11 68389949 missense variant G/A snv 1
rs121908665 1.000 0.120 11 68403606 missense variant C/T snv 1
rs121908666 1.000 0.120 11 68389921 stop gained G/T snv 1
rs121908667 1.000 0.120 11 68410024 stop gained G/A snv 7.0E-06 1
rs1219101402 1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06 1
rs1273567061 1.000 0.120 11 68386525 missense variant A/G snv 4.0E-06 2.1E-05 1
rs1318906451 1.000 0.120 11 68389900 missense variant T/A snv 4.0E-06 1
rs1470530779 1.000 0.120 11 68406769 missense variant G/A snv 4.0E-06 1
rs149645175 1.000 0.120 11 68448822 stop gained C/G;T snv 3.7E-05 1
rs1554967141 1.000 0.120 11 68389935 frameshift variant G/- delins 1
rs1554967176 1.000 0.120 11 68390053 splice donor variant G/A snv 1
rs1554971145 1.000 0.120 11 68410126 frameshift variant G/- delins 1
rs201320326 1.000 0.120 11 68386499 missense variant C/A;T snv 2.2E-04 1