Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397517065 15 34792471 missense variant G/A snv 2
rs397517071 1.000 0.040 15 34792092 missense variant A/G snv 2
rs727504379 1.000 0.040 15 34791238 missense variant A/G snv 2
rs727502886 0.925 0.040 1 236719007 missense variant G/A snv 3
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 42
rs869248137 0.882 0.120 10 119676479 stop gained C/A;T snv 4.0E-06 4
rs387906875 0.925 0.080 10 119670037 stop gained C/T snv 8.0E-06 3
rs397516881 0.827 0.120 10 119676917 missense variant G/A snv 3
rs876657634 0.925 0.080 10 119672477 stop gained C/T snv 3
rs727505109 1.000 10 119676617 frameshift variant C/- delins 2
rs1554875409 10 119651752 stop gained G/A snv 1
rs1564773559 10 119669920 frameshift variant -/TGTGTAC delins 1
rs727502897 10 119651742 frameshift variant C/-;CC delins 1
rs727505283 10 119651774 frameshift variant ACCGGCTG/- delins 1
rs730880055 10 119676851 stop gained C/T snv 1
rs869025365 10 119672657 splice donor variant G/A snv 1
rs397516784 0.925 0.080 6 118558957 inframe deletion AGA/- delins 1.4E-05 4
rs1565050320 11 19185040 missense variant C/G snv 1
rs1565053085 11 19192353 synonymous variant C/T snv 1
rs1565053147 11 19192403 missense variant T/A snv 1
rs876657767 11 19186276 missense variant C/G;T snv 1
rs267607490
DES
0.925 0.160 2 219425734 missense variant C/T snv 4
rs150974575
DES
1.000 0.160 2 219423817 stop gained C/T snv 1.2E-05 3
rs267607483
DES
1.000 0.160 2 219420349 splice region variant A/G;T snv 2
rs267607495
DES
2 219418497 missense variant C/T snv 2