Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs80338671 | 0.851 | 0.120 | 3 | 81642787 | missense variant | T/C;G | snv | 4.5E-04; 3.2E-04 | 5 | ||
rs201958741 | 0.851 | 0.120 | 3 | 81577999 | missense variant | C/T | snv | 3.3E-05 | 4.9E-05 | 4 | |
rs137852888 | 0.882 | 0.120 | 3 | 81577973 | stop gained | G/A;C | snv | 3.7E-05 | 5.6E-05 | 3 | |
rs192044702 | 0.882 | 0.120 | 3 | 81648854 | splice donor variant | A/G | snv | 8.9E-04 | 7.7E-04 | 3 | |
rs1057517315 | 0.925 | 0.080 | 3 | 81705469 | frameshift variant | T/- | delins | 2 | |||
rs137852887 | 0.925 | 0.080 | 3 | 81646403 | missense variant | A/T | snv | 1.4E-05 | 2 | ||
rs766935302 | 0.925 | 0.080 | 3 | 81535220 | stop gained | G/A;C | snv | 2.8E-05 | 2 | ||
rs80338672 | 0.925 | 0.080 | 3 | 81578000 | missense variant | G/A | snv | 3.7E-05 | 7.0E-06 | 2 |