Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555759066 0.925 0.120 19 13308496 stop gained C/T snv 2
rs1555762855 0.925 0.120 19 13317146 frameshift variant AACAATAGCAACACACAGCGTG/- delins 2
rs1555762908 0.925 0.120 19 13317228 frameshift variant C/- del 2
rs1568457080 0.925 0.120 19 13245181 splice donor variant C/A snv 2
rs1568470104 0.925 0.120 19 13259661 stop gained G/A snv 2
rs1568473233 0.925 0.120 19 13262790 stop gained G/A snv 2
rs1568528144 0.925 0.120 19 13317198 stop gained C/T snv 2
rs1568528298 0.925 0.120 19 13317254 frameshift variant -/T delins 2
rs779221807 0.925 0.120 19 13212204 stop gained G/A snv 2
rs121908227 1.000 0.120 19 13261495 missense variant A/C snv 1
rs121908228 1.000 0.120 19 13365344 missense variant G/A snv 1
rs121908229 1.000 0.120 19 13234966 missense variant T/A snv 1
rs121908231 1.000 0.120 19 13365335 missense variant A/G snv 1
rs121908232 1.000 0.120 19 13257499 missense variant C/G;T snv 4.3E-06 1
rs121908233 1.000 0.120 19 13257474 missense variant A/G snv 1
rs121908234 1.000 0.120 19 13257466 missense variant C/T snv 4.0E-06 1.4E-05 1
rs121908235 1.000 0.120 19 13209438 missense variant G/A snv 4.5E-05 6.3E-05 1
rs121908238 1.000 0.120 19 13365358 missense variant T/C snv 1
rs121908239 1.000 0.120 19 13334411 missense variant G/A snv 1
rs121908240 1.000 0.120 19 13317168 missense variant G/A snv 4.0E-06 1.4E-05 1
rs121908241 1.000 0.120 19 13299243 missense variant A/G snv 4.1E-06 1
rs121908242 1.000 0.120 19 13298946 missense variant G/A;C snv 5.6E-05; 1.1E-03 1
rs121908243 1.000 0.120 19 13235649 missense variant G/A snv 7.0E-06 1
rs121908244 1.000 0.120 19 13228722 missense variant A/G snv 1
rs121908246 1.000 0.120 19 13308123 missense variant C/A;T snv 1