Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398124401 | 0.695 | 0.480 | 4 | 55346393 | stop gained | G/A | snv | 1.2E-04 | 2.8E-05 | 26 | |
rs1555570093 | 0.807 | 0.280 | 17 | 7586699 | missense variant | G/A | snv | 12 | |||
rs1218912272 | 0.925 | 0.160 | 1 | 152314342 | stop gained | T/A | snv | 4.0E-06 | 8 | ||
rs28929485 | 0.807 | 0.320 | 13 | 20189532 | missense variant | G/A;C | snv | 7 | |||
rs111033307 | 0.851 | 0.240 | 7 | 107694473 | missense variant | T/G | snv | 1.0E-04 | 7.7E-05 | 6 | |
rs1569044747 | 0.882 | 0.120 | 22 | 37139219 | stop gained | G/A | snv | 5 | |||
rs147040026 | 0.882 | 0.120 | 3 | 48591738 | missense variant | C/G;T | snv | 4.0E-06; 1.6E-05 | 4 | ||
rs1457403673 | 0.882 | 0.120 | 17 | 41586785 | missense variant | G/A | snv | 7.0E-06 | 4 | ||
rs1373855924 | 0.851 | 0.240 | 15 | 91009812 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
rs118203937 | 0.882 | 0.080 | 19 | 15540506 | missense variant | G/A;T | snv | 3.6E-05; 4.0E-06 | 3 | ||
rs199766569 | 0.925 | 0.080 | 17 | 8075687 | missense variant | T/C | snv | 1.9E-04 | 1.4E-04 | 2 | |
rs370031870 | 0.925 | 0.080 | 17 | 8115623 | stop gained | G/A;T | snv | 2.0E-05; 4.0E-06 | 2 | ||
rs200806519 | 0.925 | 0.080 | 6 | 36291501 | missense variant | C/A;T | snv | 2.4E-05 | 4.1E-05 | 2 | |
rs1553520468 | 0.925 | 0.080 | 2 | 214955362 | splice acceptor variant | C/G | snv | 2 | |||
rs121918719 | 0.925 | 0.080 | 14 | 24261775 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 2 | |
rs863223405 | 0.925 | 0.080 | 14 | 24258324 | missense variant | A/G | snv | 2 | |||
rs780420901 | 1.000 | 0.080 | 17 | 8073215 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs1057517836 | 1.000 | 0.080 | 14 | 24261795 | stop gained | -/TACTCATACT | delins | 1 |