Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558008455 0.851 0.280 1 160135284 frameshift variant GT/- delins 4
rs1558005340 0.851 0.280 1 160127638 frameshift variant C/- del 4
rs1558003446 1.000 0.080 1 160123327 frameshift variant -/TC delins 2
rs1558010146 1.000 0.080 1 160139668 stop gained G/T snv 2
rs121918615 0.925 0.040 1 160139735 missense variant C/T snv 2
rs1553245943 1.000 0.080 1 160137001 missense variant G/A snv 2
rs1553245178 1 160130548 missense variant G/A snv 1
rs1553245857 1.000 0.040 1 160136370 missense variant G/A snv 1
rs1553245771 0.882 0.040 1 160135461 missense variant G/A snv 1
rs1226796744 1.000 0.040 1 160139675 missense variant C/T snv 4.0E-06 2.1E-05 1
rs1165052640 1.000 0.040 1 160129024 stop gained C/T snv 4.1E-06 7.0E-06 1
rs149144720 1.000 0.040 1 160136570 missense variant G/A snv 1
rs1558008759 1.000 0.040 1 160135988 missense variant G/C snv 1
rs121918614 1.000 0.040 1 160135470 missense variant G/A snv 7.0E-06 1
rs869025341 1.000 0.040 1 160124371 missense variant G/A snv 1
rs28933400 0.882 0.080 1 160135510 missense variant T/C snv 1
rs28933399 1.000 0.040 1 160136665 missense variant T/C snv 1
rs28933398 1.000 0.040 1 160135845 missense variant T/C snv 1
rs121918617 1.000 0.040 1 160127660 missense variant T/C snv 7.0E-06 1
rs121918612 0.925 0.040 1 160127704 missense variant G/A snv 1
rs121918620 1.000 0.040 1 160128761 missense variant C/G;T snv 1
rs121918613 0.925 0.080 1 160128667 missense variant A/G snv 1
rs28933401 0.882 0.120 1 160135246 missense variant G/A snv 1
rs121918616 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 1
rs28934002 1.000 1 160128767 missense variant C/A;T snv 1