Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1315533129 1.000 0.120 19 13285067 splice donor variant C/A;T snv 4.1E-06 1
rs1555762869 1.000 0.120 19 13317187 frameshift variant TG/- del 1
rs1568473171 1.000 0.120 19 13262772 stop gained G/A snv 1
rs1568514371 1.000 0.120 19 13303803 frameshift variant AG/CTCC delins 1
rs587776692 1.000 0.120 19 13283295 frameshift variant G/- delins 1
rs587776693 1.000 0.120 19 13275849 splice donor variant C/T snv 1
rs587776694 1.000 0.120 19 13298819 frameshift variant -/C delins 1
rs587776695 1.000 0.120 19 13253015 frameshift variant C/- del 1
rs746790849 1.000 0.120 19 13286645 frameshift variant G/-;GG delins 1