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 |