Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs587777585 | 0.882 | 6 | 30918851 | missense variant | C/G;T | snv | 2.4E-05 | 6 | |||
rs1057516049 | 0.851 | 0.040 | 8 | 41933963 | frameshift variant | CACT/- | delins | 7 | |||
rs730882147 | 0.851 | 0.080 | 6 | 41909351 | missense variant | C/G | snv | 7.0E-06 | 5 | ||
rs895293055 | 0.851 | 0.080 | 6 | 41909351 | frameshift variant | C/- | delins | 5 | |||
rs879253798 | 1.000 | 0.080 | 16 | 89524099 | frameshift variant | TC/- | delins | 3 | |||
rs886041091 | 0.807 | 0.120 | 9 | 84751990 | missense variant | A/G | snv | 18 | |||
rs672601369 | 0.790 | 0.120 | 2 | 240783780 | missense variant | C/T | snv | 10 | |||
rs1060502227 | 0.851 | 0.120 | 2 | 32136593 | missense variant | C/G;T | snv | 6 | |||
rs1555471098 | 0.925 | 0.120 | 16 | 3728852 | frameshift variant | GCTGGGTGAGA/- | del | 6 | |||
rs1057519087 | 0.925 | 0.120 | 1 | 39967632 | missense variant | C/T | snv | 7.0E-06 | 4 | ||
rs138490803 | 0.925 | 0.120 | 16 | 19074000 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 3 | |
rs864321686 | 0.925 | 0.120 | 16 | 19075775 | missense variant | T/A | snv | 3 | |||
rs375817528 | 0.776 | 0.160 | 11 | 65206824 | splice region variant | G/A | snv | 1.2E-04 | 1.2E-04 | 25 | |
rs1217391623 | 0.882 | 0.160 | 16 | 89556976 | frameshift variant | G/- | del | 7.0E-06 | 11 | ||
rs104894107 | 0.882 | 0.160 | 9 | 69064942 | missense variant | G/C;T | snv | 3.6E-05; 2.8E-05 | 6 | ||
rs121918358 | 0.882 | 0.160 | 16 | 89510539 | stop gained | T/A | snv | 4.2E-04 | 1.8E-04 | 5 | |
rs141659620 | 0.882 | 0.160 | 16 | 89531961 | missense variant | G/A;C | snv | 8.3E-04; 8.0E-06 | 5 | ||
rs72547551 | 0.882 | 0.160 | 16 | 89550545 | missense variant | C/T | snv | 3.6E-05 | 1.5E-04 | 5 | |
rs748309520 | 0.882 | 0.160 | 16 | 89531903 | splice acceptor variant | G/A | snv | 1.6E-05 | 7.0E-06 | 5 | |
rs752989523 | 0.882 | 0.160 | 16 | 89553853 | stop gained | G/A;C | snv | 8.0E-06 | 5 | ||
rs879253797 | 0.882 | 0.160 | 16 | 89556954 | missense variant | C/T | snv | 1.4E-05 | 5 | ||
rs1555731819 | 0.807 | 0.200 | 19 | 35729980 | missense variant | G/T | snv | 26 | |||
rs387906799 | 0.742 | 0.200 | 2 | 240788118 | missense variant | G/A | snv | 19 | |||
rs776679653 | 0.827 | 0.200 | 9 | 86266174 | missense variant | C/T | snv | 4.2E-06 | 11 | ||
rs80338700 | 0.851 | 0.200 | 16 | 8806398 | missense variant | C/G;T | snv | 4.0E-06; 2.4E-05 | 7 |