Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3218716 | 0.716 | 0.280 | 14 | 23425316 | missense variant | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 17 | ||
rs587777630 | 0.716 | 0.440 | 2 | 190986921 | missense variant | G/A | snv | 16 | |||
rs74315329 | 0.732 | 0.240 | 1 | 171636338 | stop gained | G/A | snv | 1.1E-03 | 8.7E-04 | 15 | |
rs1426488816 | 0.827 | 0.160 | 9 | 26913948 | splice acceptor variant | C/T | snv | 8.0E-06 | 9 | ||
rs1555908409 | 0.851 | 0.160 | 22 | 37232842 | missense variant | C/T | snv | 7 | |||
rs199840952 | 0.827 | 0.240 | 2 | 97732893 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 7 | |
rs869025224 | 0.827 | 0.240 | 2 | 97734709 | missense variant | G/C | snv | 7.0E-06 | 7 | ||
rs750610248 | 0.882 | 0.200 | 14 | 99175513 | missense variant | A/C;G | snv | 4.1E-06 | 3 | ||
rs1567629968 | 0.882 | 0.160 | 16 | 67648973 | missense variant | C/A | snv | 3 | |||
rs863225436 | 0.925 | 0.120 | 3 | 196075339 | missense variant | A/G | snv | 2 | |||
rs1437892966 | 1.000 | 0.120 | 10 | 14945140 | missense variant | T/G | snv | 7.0E-06 | 1 |