Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519915 | 0.851 | 0.160 | 1 | 11109318 | missense variant | A/C | snv | 5 | |||
rs1057519914 | 0.851 | 0.240 | 1 | 11157174 | missense variant | A/G | snv | 4 | |||
rs1057519916 | 0.882 | 0.160 | 1 | 11109320 | missense variant | T/A | snv | 4 | |||
rs786205165 | 0.882 | 0.120 | 1 | 11157173 | missense variant | C/A;T | snv | 4 | |||
rs1057519913 | 0.925 | 0.120 | 1 | 11157172 | missense variant | G/C | snv | 3 |