Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1010184002 | 0.689 | 0.400 | 6 | 42978878 | stop gained | C/T | snv | 7.0E-06 | 60 | ||
rs137854889 | 0.742 | 0.440 | 1 | 40290871 | frameshift variant | T/-;TT | delins | 31 | |||
rs1555038111 | 0.701 | 0.480 | 11 | 118478153 | stop gained | T/G | snv | 37 | |||
rs1563183492 | 0.708 | 0.520 | 7 | 70766248 | missense variant | C/T | snv | 32 | |||
rs1569355102 | 0.695 | 0.360 | 21 | 37472869 | frameshift variant | TAAC/- | delins | 51 | |||
rs3135718 | 0.882 | 0.160 | 10 | 121594355 | intron variant | C/T | snv | 0.54 | 4 | ||
rs373145711 | 0.732 | 0.520 | 20 | 32433408 | stop gained | C/T | snv | 2.0E-05 | 2.8E-05 | 25 | |
rs61753219 | 0.672 | 0.400 | 6 | 42978330 | missense variant | G/A | snv | 3.6E-05 | 2.8E-05 | 64 | |
rs756096100 | 1.000 | 0.080 | 4 | 5568481 | missense variant | C/A;G;T | snv | 4.9E-06; 4.9E-06 | 1 | ||
rs863223330 | 0.807 | 0.280 | 14 | 60648629 | splice donor variant | C/G | snv | 8 | |||
rs864309486 | 0.763 | 0.320 | 6 | 24777262 | stop gained | A/T | snv | 21 | |||
rs864309487 | 0.763 | 0.280 | 6 | 24777279 | frameshift variant | TCAA/- | delins | 20 | |||
rs886041065 | 0.677 | 0.600 | 2 | 25743913 | frameshift variant | G/- | delins | 43 |