Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs796052019 0.882 0.160 13 100157297 missense variant G/A;T snv 4.0E-06 3
rs1242465339 1.000 0.080 19 29207763 stop gained G/A;T snv 7.0E-06 3
rs1568344751 1.000 0.080 19 29208159 splice acceptor variant C/G snv 3
rs1568346416 1.000 0.080 19 29213078 missense variant A/T snv 3
rs202247814 1.000 0.080 13 100155090 missense variant G/A snv 2
rs1389933015 1.000 0.080 13 100530089 intron variant A/G snv 1.4E-05 1
rs199604072 1.000 0.080 13 100330672 splice donor variant G/C;T snv 4.0E-06 1
rs118169528 1.000 0.080 13 100368504 missense variant G/T snv 3.0E-03 9.1E-04 1
rs1194679272 1.000 0.080 13 100449261 stop gained C/T snv 1.3E-05 1
rs121964957 1.000 0.080 13 100268731 stop gained A/C;G;T snv 6.4E-05; 4.0E-06 1
rs121964958 1.000 0.080 13 100301512 missense variant T/A snv 4.0E-06 7.0E-06 1
rs1241896966 1.000 0.080 13 100527690 stop gained G/T snv 7.0E-06 1
rs1301904623 1.000 0.080 13 100301590 missense variant G/A snv 8.0E-06 7.0E-06 1
rs138149179 1.000 0.080 13 100273218 stop gained C/T snv 3.6E-05 2.8E-05 1
rs141371306 1.000 0.080 13 100111886 missense variant C/T snv 2.0E-05 5.6E-05 1
rs1443858896 1.000 0.080 13 100302982 missense variant C/T snv 8.0E-06 1
rs1467680142 1.000 0.080 13 100301606 splice region variant A/G snv 4.0E-06 1
rs1555298451 1.000 0.080 13 100449251 splice acceptor variant G/A snv 1
rs1555327702 1.000 0.080 13 100515553 frameshift variant A/- delins 1
rs1555327732 1.000 0.080 13 100515568 splice donor variant G/T snv 1
rs1555331314 1.000 0.080 13 100527737 frameshift variant T/- del 1
rs1555342593 1.000 0.080 13 100102962 splice donor variant T/C snv 1
rs1555361758 1.000 0.080 13 100157312 frameshift variant C/- del 1
rs1555400381 1.000 0.080 13 100268712 frameshift variant T/- del 1
rs202247815 1.000 0.080 13 100209354 missense variant T/C snv 4.0E-06 1