Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs151340631 | 0.925 | 0.240 | X | 78011216 | stop gained | C/G;T | snv | 1 | |||
rs151340632 | 0.925 | 0.240 | X | 78042694 | missense variant | A/G | snv | 1 | |||
rs367775730 | 1.000 | 0.160 | X | 78015786 | missense variant | G/A | snv | 2.1E-04 | 8.5E-05 | 1 | |
rs72554639 | 1.000 | 0.160 | X | 78011191 | missense variant | G/C | snv | 1 | |||
rs72554642 | 1.000 | 0.160 | X | 78011619 | missense variant | T/G | snv | 1 | |||
rs72554644 | 1.000 | 0.160 | X | 78012885 | stop gained | G/A;T | snv | 1 | |||
rs72554646 | 1.000 | 0.160 | X | 78015873 | missense variant | T/G | snv | 1 | |||
rs72554651 | 1.000 | 0.160 | X | 78029350 | missense variant | T/C | snv | 1 | |||
rs72554652 | 1.000 | 0.160 | X | 78029389 | missense variant | G/A | snv | 1 | |||
rs72554654 | 1.000 | 0.160 | X | 78033663 | missense variant | G/A | snv | 1 | |||
rs72554655 | 1.000 | 0.160 | X | 78040695 | missense variant | G/A | snv | 1 | |||
rs72554657 | 1.000 | 0.160 | X | 78042687 | missense variant | G/A | snv | 1 | |||
rs797045390 | 1.000 | 0.160 | X | 78042726 | missense variant | G/A | snv | 1 |