Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs421016 | 0.683 | 0.440 | 1 | 155235252 | missense variant | A/C;G | snv | 8.0E-06; 1.3E-03 | 30 | ||
rs761807915 | 0.925 | 0.120 | 20 | 4699824 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 4 | |
rs772784579 | 1.000 | 0.040 | 17 | 44352387 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs1336432413 | 1.000 | 0.040 | 10 | 69171174 | stop gained | A/T | snv | 1 | |||
rs745601645 | 1.000 | 0.040 | 10 | 69157111 | missense variant | A/G | snv | 1.6E-05 | 1 | ||
rs1443067262 | 1.000 | 0.040 | 11 | 134235007 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 |