Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs759452074 | 0.925 | 0.200 | 22 | 50523835 | missense variant | C/A;T | snv | 8.0E-06; 3.2E-05 | 2 | ||
rs74315511 | 0.925 | 0.240 | 22 | 50523994 | missense variant | C/T | snv | 8.0E-05 | 1.1E-04 | 2 | |
rs1352878283 | 1.000 | 0.120 | 22 | 50523639 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs370130010 | 1.000 | 0.040 | 22 | 50524078 | missense variant | G/A;T | snv | 4.8E-05 | 1 | ||
rs375954523 | 1.000 | 0.040 | 22 | 50524054 | missense variant | G/A;T | snv | 8.0E-05; 4.0E-06 | 1 | ||
rs145100473 | 1.000 | 0.040 | 22 | 50524071 | missense variant | C/T | snv | 8.3E-04 | 7.6E-04 | 1 | |
rs8139305 | 1.000 | 0.040 | 22 | 50523636 | missense variant | G/A;T | snv | 2.4E-03; 4.0E-06 | 1 | ||
rs28937868 | 1.000 | 0.200 | 22 | 50524014 | missense variant | C/T | snv | 1 | |||
rs28937598 | 1.000 | 0.200 | 22 | 50523901 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs80358232 | 1.000 | 0.200 | 22 | 50523738 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs149977726 | 1.000 | 22 | 50527265 | missense variant | T/C | snv | 1.2E-05 | 9.8E-05 | 1 |