Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113019349 0.925 0.120 11 6616004 splice donor variant C/G;T snv 2
rs119455954 0.925 0.120 11 6616056 missense variant C/T snv 1.6E-05 4.9E-05 2
rs119455955 0.851 0.120 11 6617040 stop gained G/A snv 2.2E-04 2.4E-04 4
rs119455957 0.882 0.120 11 6616696 missense variant C/A snv 8.0E-06 7.0E-06 3
rs121908199 0.925 0.120 11 6615542 missense variant C/T snv 2
rs121908200 0.925 0.120 11 6615442 missense variant C/G snv 2.0E-05 2.1E-05 2
rs121908202 0.925 0.120 11 6615172 missense variant G/A snv 2.4E-05 2
rs121908209 0.925 0.120 11 6617045 missense variant C/G;T snv 4.0E-06; 4.0E-06 2
rs1554902052 0.925 0.120 11 6617430 splice acceptor variant T/C snv 2
rs1564855725 0.882 0.160 11 6617621 splice region variant C/T snv 5
rs202189057 0.925 0.120 11 6617695 stop gained A/T snv 4.0E-06 2
rs56144125 0.827 0.240 11 6617154 splice acceptor variant C/A;G;T snv 4.0E-04; 1.2E-05 6
rs756564767 0.882 0.120 11 6617627 stop gained G/A snv 6.4E-05 4.2E-05 3
rs763162812 0.925 0.120 11 6616720 missense variant T/A snv 1.6E-05 2.8E-05 2
rs765380155 0.925 0.120 11 6616374 missense variant C/T snv 4.0E-06 1.4E-05 2
rs786204753 0.925 0.120 11 6615217 stop gained C/T snv 2
rs1554902216 0.925 0.120 11 6618820 frameshift variant AG/- delins 2