Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs886041065 | 0.677 | 0.600 | 2 | 25743913 | frameshift variant | G/- | delins | 43 | |||
rs866294686 | 0.683 | 0.480 | 10 | 102657073 | stop gained | C/A;T | snv | 43 | |||
rs121912504 | 0.851 | 0.200 | 7 | 150951711 | missense variant | G/A | snv | 6 | |||
rs1554430943 | 0.925 | 0.160 | 7 | 150974821 | missense variant | C/T | snv | 4 | |||
rs1554919471 | 0.925 | 0.200 | 11 | 2768861 | frameshift variant | G/- | delins | 4 | |||
rs758346045 | 1.000 | 0.080 | 21 | 34449497 | stop gained | G/A;T | snv | 2.0E-05; 8.0E-06 | 3 | ||
rs120074185 | 0.925 | 0.120 | 11 | 2776032 | missense variant | C/A;T | snv | 1.1E-05; 1.1E-05 | 3 | ||
rs1554920808 | 1.000 | 0.120 | 11 | 2776991 | missense variant | A/G | snv | 3 | |||
rs1554958045 | 1.000 | 0.080 | 11 | 2445213 | stop gained | G/T | snv | 3 | |||
rs199472706 | 0.925 | 0.120 | 11 | 2571391 | missense variant | C/T | snv | 4.0E-06 | 1.0E-04 | 3 | |
rs199473442 | 1.000 | 0.120 | 11 | 2445103 | missense variant | C/G;T | snv | 3 | |||
rs1564821090 | 11 | 2572850 | missense variant | T/C | snv | 1 |