Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs746442213 | 1.000 | 0.040 | 2 | 29232307 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
rs199897804 | 1.000 | 0.040 | X | 18604645 | missense variant | C/A;T | snv | 4.9E-05 | 1 | ||
rs1279653488 | 1.000 | 0.040 | 17 | 64047898 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
rs1411105125 | 1.000 | 0.040 | 19 | 12873875 | missense variant | C/T | snv | 1 | |||
rs540521894 | 1.000 | 0.040 | 1 | 156864760 | missense variant | C/A;T | snv | 4.0E-06; 5.6E-05 | 2.1E-05 | 1 | |
rs190220654 | 1.000 | 0.040 | 10 | 104002988 | missense variant | G/C | snv | 1.2E-04 | 4.2E-05 | 1 | |
rs1490428165 | 1.000 | 0.040 | 9 | 27209192 | missense variant | C/G;T | snv | 4.0E-06 | 1 |