Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1553592703 1.000 0.040 2 222294222 frameshift variant -/AG ins 1
rs1553572967 0.925 0.040 2 222221300 frameshift variant -/C delins 2
rs1553592713 1.000 0.040 2 222294228 frameshift variant -/T delins 1
rs1553594009 1.000 0.040 2 222297162 frameshift variant -/T delins 1
rs1553568831 1.000 0.040 2 222201988 frameshift variant -/TGTA delins 1
rs1553575191 1.000 0.040 2 222232178 missense variant A/G snv 1
rs1553575179 1.000 0.040 2 222232131 frameshift variant AATGTCAGGGTAA/- delins 1
rs1559320252 1.000 0.040 2 222297018 frameshift variant AGTCTCCTGGTACC/- delins 1
rs1553592757 1.000 0.040 2 222294269 frameshift variant ATT/TA delins 1
rs1553572946 1.000 0.040 2 222221259 frameshift variant C/- del 1
rs1553592766 1.000 0.040 2 222294289 frameshift variant C/- del 1
rs1553593917 1.000 0.040 2 222297067 missense variant C/A snv 1
rs267606931 1.000 0.040 2 222297132 missense variant C/A snv 1
rs773327091 1.000 0.040 2 222297175 missense variant C/A;G snv 1
rs1419548558 1.000 0.040 2 222297157 missense variant C/A;G;T snv 1
rs587776586 1.000 0.040 2 222297057 missense variant C/G snv 1
rs1020175890 1.000 0.040 2 222221362 missense variant C/T snv 1
rs1189463428 1.000 0.040 2 222297003 missense variant C/T snv 1
rs774528745 1.000 0.040 2 222221368 missense variant C/T snv 1
rs1559318562 1.000 0.040 2 222295610 frameshift variant CTTTT/- delins 1
rs1559316542 1.000 0.040 2 222294197 frameshift variant G/- del 1
rs104893651 0.925 0.040 2 222297048 missense variant G/A snv 2
rs1228590199 0.925 0.040 2 222221372 missense variant G/A snv 4.0E-06 7.0E-06 2
rs104893650 1.000 0.040 2 222297150 missense variant G/A snv 1
rs1380858784 1.000 0.040 2 222221369 missense variant G/A snv 1