Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137852986 | 0.732 | 0.440 | 17 | 61716051 | stop gained | G/A | snv | 1.7E-04 | 1.5E-04 | 13 | |
rs4968451 | 0.732 | 0.160 | 17 | 61849946 | intron variant | A/C | snv | 0.15 | 13 | ||
rs4986764 | 0.827 | 0.120 | 17 | 61685986 | missense variant | A/G | snv | 0.60 | 0.61 | 8 | |
rs2048718 | 0.827 | 0.120 | 17 | 61863458 | 5 prime UTR variant | C/T | snv | 0.42 | 5 | ||
rs11871753 | 0.851 | 0.120 | 17 | 61779284 | intron variant | A/G | snv | 0.75 | 4 | ||
rs16945628 | 0.851 | 0.120 | 17 | 61789868 | intron variant | T/C | snv | 0.60 | 4 | ||
rs7220719 | 0.882 | 0.120 | 17 | 61736921 | intron variant | A/G | snv | 0.73 | 3 | ||
rs1555616176 | 0.925 | 0.080 | 17 | 61849196 | frameshift variant | T/- | del | 2 | |||
rs4988349 | 0.925 | 0.080 | 17 | 61784279 | missense variant | T/A | snv | 3.6E-05 | 2.8E-05 | 2 | |
rs769797684 | 0.925 | 0.080 | 17 | 61744510 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 2 |