Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs28934872 | 0.851 | 0.200 | 16 | 2070571 | missense variant | G/A | snv | 5 | |||
rs45469298 | 0.851 | 0.200 | 16 | 2070570 | missense variant | C/G;T | snv | 5 | |||
rs45517305 | 0.851 | 0.240 | 16 | 2081646 | stop gained | C/A;T | snv | 5 | |||
rs45517412 | 0.882 | 0.200 | 16 | 2088293 | missense variant | C/G;T | snv | 4 | |||
rs45517395 | 0.882 | 0.200 | 16 | 2088117 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
rs1131691965 | 0.882 | 0.200 | 16 | 2074394 | splice region variant | G/C | snv | 3 | |||
rs1567387207 | 0.882 | 0.200 | 16 | 2050487 | splice donor variant | G/A | snv | 3 | |||
rs1567437155 | 0.882 | 0.200 | 16 | 2064286 | frameshift variant | C/- | del | 3 | |||
rs1567489890 | 1.000 | 0.120 | 16 | 2077476 | non coding transcript exon variant | G/A | snv | 3 | |||
rs45517179 | 0.882 | 0.200 | 16 | 2064341 | stop gained | C/G;T | snv | 3 | |||
rs45517222 | 0.882 | 0.200 | 16 | 2072879 | stop gained | C/T | snv | 3 | |||
rs45517259 | 0.925 | 0.120 | 16 | 2076142 | missense variant | G/A | snv | 3 | |||
rs773920155 | 0.925 | 0.120 | 16 | 2061946 | stop gained | G/A;T | snv | 4.0E-06 | 3 | ||
rs137854218 | 0.925 | 0.120 | 16 | 2088293 | inframe insertion | CATCAAGCGGCTCCGCCA/-;CATCAAGCGGCTCCGCCACATCAAGCGGCTCCGCCA | delins | 3 | |||
rs45507199 | 0.925 | 0.120 | 16 | 2088294 | missense variant | G/A;C;T | snv | 3 | |||
rs1060500931 | 0.925 | 0.120 | 16 | 2064302 | stop gained | C/T | snv | 2 | |||
rs397514916 | 0.925 | 0.120 | 16 | 2083754 | missense variant | C/G;T | snv | 2 | |||
rs397515297 | 1.000 | 0.120 | 16 | 2064275 | stop gained | G/A;T | snv | 2 | |||
rs45438205 | 0.925 | 0.120 | 16 | 2080365 | missense variant | C/T | snv | 7.0E-06 | 2 | ||
rs45451497 | 1.000 | 0.120 | 16 | 2080179 | stop gained | C/T | snv | 2 | |||
rs45483392 | 0.925 | 0.120 | 16 | 2087897 | missense variant | C/A;T | snv | 2 | |||
rs45486196 | 1.000 | 0.120 | 16 | 2071924 | missense variant | G/A | snv | 2 | |||
rs45487497 | 0.925 | 0.120 | 16 | 2058779 | missense variant | G/A | snv | 2 | |||
rs45516293 | 0.925 | 0.120 | 16 | 2084965 | missense variant | A/C;G | snv | 2 | |||
rs45517099 | 1.000 | 0.120 | 16 | 2053384 | stop gained | C/T | snv | 2 |