Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060502164 1.000 0.080 1 115744914 splice acceptor variant T/C snv 1
rs139228801 1.000 0.080 1 115705208 missense variant G/A;T snv 3.2E-05 1
rs146664754 1.000 0.080 1 115732940 missense variant G/C snv 7.2E-04 5.4E-04 1
rs151115064 1.000 0.080 1 115725543 missense variant G/A snv 5.3E-05 7.9E-05 1
rs397507555 1.000 0.080 1 115768480 frameshift variant T/- del 1
rs397507556 1.000 0.080 1 115768445 stop gained G/A;T snv 4.0E-06; 1.6E-05 1
rs397516643 1.000 0.080 1 115732927 frameshift variant TGA/GT delins 1
rs763955301 1.000 0.080 1 115732961 frameshift variant A/- delins 7.0E-06 1
rs876657635 1.000 0.080 1 115702996 splice acceptor variant C/A snv 1
rs199473368 1.000 0.080 17 70175239 missense variant G/A snv 1
rs199473657 1.000 0.080 17 70175718 missense variant G/T snv 1
rs765542241 1.000 0.080 7 92234838 missense variant T/C snv 6.4E-05 1.4E-05 1
rs1554258777 1.000 0.080 6 123570921 splice donor variant A/T snv 1
rs1060500137 1.000 0.080 1 237772077 missense variant G/A snv 1
rs1060500142 1.000 0.080 1 237330939 missense variant C/T snv 4.0E-06 1
rs1185619003 1.000 0.080 1 237830557 missense variant A/G snv 1
rs1188352725 1.000 0.080 1 237798091 missense variant G/C snv 1
rs1202962809 1.000 0.080 1 237784184 missense variant A/C snv 1
rs1218096653 1.000 0.080 1 237828391 missense variant T/G snv 1
rs1234963411 1.000 0.080 1 237784188 missense variant A/C snv 1
rs1235005255 1.000 0.080 1 237648548 missense variant T/A snv 1
rs1239093704 1.000 0.080 1 237759849 missense variant G/T snv 4.0E-06 1
rs1242723821 1.000 0.080 1 237828429 missense variant T/C snv 1
rs1323621379 1.000 0.080 1 237791464 missense variant G/A snv 1
rs1349176732 1.000 0.080 1 237445485 missense variant A/T snv 1