Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs200034765 | 10 | 69247416 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 1 | |||
rs201306926 | 4 | 140399004 | missense variant | T/C | snv | 3.6E-05 | 7.0E-06 | 1 | |||
rs201435914 | 19 | 53636878 | stop gained | C/T | snv | 3.5E-04 | 3.6E-04 | 1 | |||
rs201805961 | 20 | 25292483 | missense variant | A/G | snv | 2.4E-05 | 2.1E-05 | 1 | |||
rs202070666 | X | 154460239 | missense variant | G/A | snv | 2.2E-04 | 6.5E-04 | 1 | |||
rs370433088 | 20 | 62322314 | missense variant | C/T | snv | 1.0E-04 | 1.0E-04 | 1 | |||
rs375633720 | 4 | 8601494 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 1 | |||
rs376253982 | X | 48966313 | splice region variant | C/A | snv | 2.0E-04 | 2.1E-04 | 1 | |||
rs377035972 | 14 | 24155679 | missense variant | G/A | snv | 5.6E-05 | 9.8E-05 | 1 | |||
rs377314861 | 18 | 21440307 | missense variant | C/T | snv | 6.3E-06 | 1 | ||||
rs537353127 | 11 | 61273265 | stop gained | G/A;C;T | snv | 4.0E-06; 4.0E-06; 8.0E-06 | 1 | ||||
rs540351799 | 1 | 29325243 | missense variant | A/C | snv | 1.2E-05 | 1.4E-05 | 1 | |||
rs559634261 | 1 | 39318497 | missense variant | G/A | snv | 2.0E-05 | 1 | ||||
rs559788899 | 1 | 29303909 | missense variant | C/T | snv | 2.8E-05 | 1.4E-05 | 1 | |||
rs746040003 | 13 | 114018810 | frameshift variant | TCAG/- | delins | 1.6E-05 | 1 | ||||
rs747141054 | 8 | 42973316 | missense variant | G/A | snv | 2.4E-05 | 4.9E-05 | 1 | |||
rs747262678 | 1 | 228279343 | missense variant | C/T | snv | 1.2E-05 | 1.4E-05 | 1 | |||
rs747762087 | 3 | 73384465 | missense variant | T/A;G | snv | 7.0E-06 | 1 | ||||
rs747867083 | 1 | 19119624 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 1 | |||
rs748323629 | 1 | 19151825 | missense variant | T/C | snv | 8.0E-06 | 2.8E-05 | 1 | |||
rs752482499 | 14 | 23140529 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |||
rs755081350 | 1 | 39485559 | missense variant | G/A | snv | 1.6E-05 | 1 | ||||
rs756386867 | X | 38160977 | missense variant | C/G | snv | 1.1E-05 | 9.5E-06 | 1 | |||
rs759951698 | 14 | 23139485 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 1 | |||
rs760297650 | 17 | 40022789 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 1 |