Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909250 | 1.000 | 0.040 | 13 | 110719736 | missense variant | G/C | snv | 1 | |||
rs121909251 | 1.000 | 0.040 | 13 | 110719739 | missense variant | A/G | snv | 1 | |||
rs121909252 | 1.000 | 0.040 | 13 | 110719667 | missense variant | C/A | snv | 1 |