Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1029888196 | 1.000 | 0.080 | X | 15556127 | missense variant | C/T | snv | 5.7E-06 | 9.5E-06 | 1 | |
rs1239950009 | 1.000 | 0.080 | 5 | 111484451 | missense variant | C/G | snv | 1 | |||
rs1383995916 | 1.000 | 0.080 | 2 | 178589623 | missense variant | A/T | snv | 7.0E-06 | 1 | ||
rs147940573 | 1.000 | 0.080 | 7 | 98191915 | missense variant | G/A;C | snv | 7.6E-05; 2.4E-05 | 1 | ||
rs370187232 | 1.000 | 0.080 | 22 | 25772410 | missense variant | C/T | snv | 7.6E-05 | 2.0E-04 | 1 | |
rs753661271 | 1.000 | 0.080 | 7 | 98976613 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs780180192 | 1.000 | 0.080 | 22 | 26027636 | missense variant | C/G;T | snv | 4.0E-06; 8.9E-05 | 1 |