Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398122965 | 0.807 | 0.280 | 16 | 2496872 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 13 | |
rs398122967 | 0.827 | 0.280 | 16 | 2498262 | frameshift variant | T/- | del | 7.4E-05 | 4.9E-05 | 12 | |
rs376712059 | 0.827 | 0.280 | 16 | 2496605 | stop gained | G/A;C;T | snv | 6.9E-05; 8.1E-06; 4.1E-06 | 5 | ||
rs1057524191 | 0.925 | 0.040 | 16 | 2496269 | stop gained | C/T | snv | 3 | |||
rs1555501140 | 0.925 | 0.040 | 16 | 2496319 | frameshift variant | C/- | delins | 3 | |||
rs1567413218 | 0.925 | 0.040 | 16 | 2498385 | stop gained | C/G | snv | 3 | |||
rs483352866 | 0.882 | 0.240 | 16 | 2496681 | missense variant | C/G;T | snv | 8.0E-06 | 3 | ||
rs747538224 | 0.925 | 0.040 | 16 | 2496993 | missense variant | C/G | snv | 1.8E-04 | 2.1E-05 | 3 | |
rs1567411469 | 0.925 | 16 | 2496494 | stop gained | A/T | snv | 2 | ||||
rs1555501320 | 1.000 | 16 | 2497067 | missense variant | A/C | snv | 1 |