Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267606695 | 1.000 | 0.160 | 8 | 60266044 | missense variant | A/C;G | snv | 5 | |||
rs58332872 | 0.882 | 0.080 | 8 | 24956248 | missense variant | C/T | snv | 5 | |||
rs587777343 | 0.925 | 0.120 | 16 | 682232 | missense variant | C/T | snv | 5 | |||
rs752989523 | 0.882 | 0.160 | 16 | 89553853 | stop gained | G/A;C | snv | 8.0E-06 | 5 | ||
rs773372123 | 0.851 | 0.160 | 16 | 1587209 | missense variant | C/T | snv | 2.0E-05 | 5 | ||
rs104894699 | 0.925 | 0.120 | 19 | 50323694 | missense variant | C/T | snv | 4 | |||
rs1057518011 | 1 | 1535766 | missense variant | C/T | snv | 4 | |||||
rs121908214 | 0.925 | 0.080 | 19 | 13230185 | missense variant | T/G | snv | 4 | |||
rs121918514 | 0.925 | 0.080 | 19 | 53889705 | missense variant | G/A | snv | 4 | |||
rs1269252748 | 9 | 2641436 | missense variant | C/T | snv | 4 | |||||
rs1335702493 | 0.925 | 0.200 | 9 | 32973507 | stop gained | C/A;T | snv | 4 | |||
rs142157346 | 0.882 | 0.160 | 9 | 69053240 | missense variant | G/T | snv | 4 | |||
rs1563945076 | 0.925 | 0.160 | 9 | 32974556 | frameshift variant | A/- | del | 4 | |||
rs1565339091 | 1.000 | 0.200 | 11 | 124924796 | missense variant | T/C | snv | 4 | |||
rs28933381 | 0.925 | 0.080 | 12 | 4912102 | missense variant | G/C | snv | 4 | |||
rs374434303 | 0.882 | 0.200 | 19 | 7561509 | missense variant | C/A;T | snv | 3.8E-05 | 4 | ||
rs531630376 | 1.000 | 0.080 | 5 | 141955844 | stop gained | C/A | snv | 4.0E-06 | 4 | ||
rs781934508 | 1.000 | 0.080 | 9 | 133352441 | splice region variant | C/A;T | snv | 2.4E-05 | 4 | ||
rs80358243 | 0.925 | 0.200 | 22 | 50083183 | intron variant | A/G;T | snv | 8.0E-06 | 4 | ||
rs863224229 | 0.925 | 0.200 | 9 | 133356441 | start lost | ACCGCCGCCATCGCACCCGGCCCC/- | delins | 4 | |||
rs1057518796 | 1.000 | 6 | 33443751 | frameshift variant | C/- | delins | 3 | ||||
rs1057518936 | 0.925 | 0.120 | 19 | 7541025 | missense variant | C/G | snv | 3 | |||
rs118204095 | 1.000 | 0.160 | 11 | 119091414 | missense variant | G/A;T | snv | 4.5E-05 | 3 | ||
rs118204096 | 1.000 | 0.160 | 11 | 119091432 | missense variant | G/A | snv | 3 | |||
rs1208917022 | 1.000 | 0.040 | 12 | 6936663 | missense variant | A/G | snv | 3 |