RCCD1
RCC1 domain containing 1
Summary
Predicted to be involved in chromatin organization. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs758067277 | 15:91,499,990 | G/C | — | uncertain significance |
| rs2543200448 | 15:91,499,994 | C/A | — | uncertain significance |
| rs1261421714 | 15:91,499,996 | G/C | — | uncertain significance |
| rs904796415 | 15:91,500,000 | C/G | — | uncertain significance |
| rs758991986 | 15:91,500,057 | C/A | — | uncertain significance |
| rs763800846 | 15:91,500,435 | C/T | — | uncertain significance |
| rs950064029 | 15:91,500,461 | A/C | — | uncertain significance |
| rs375163894 | 15:91,500,468 | G/A | — | uncertain significance |
| rs202063703 | 15:91,500,475 | C/A | — | uncertain significance |
| rs2543202755 | 15:91,500,526 | C/T | — | uncertain significance |
| rs376583483 | 15:91,500,532 | C/T | — | uncertain significance |
| rs146488462 | 15:91,500,554 | C/T | — | benign |
| rs1324346014 | 15:91,500,594 | G/A | — | uncertain significance |
| rs1480462891 | 15:91,500,621 | C/T | — | uncertain significance |
| rs547525240 | 15:91,500,633 | C/T | — | uncertain significance |
| rs1596252586 | 15:91,500,662 | G/C | — | uncertain significance |
| rs1481455365 | 15:91,500,865 | G/A | — | uncertain significance |
| rs746579731 | 15:91,500,877 | C/A | — | uncertain significance |
| rs1105291 | 15:91,502,383 | C/A | — | — |
| rs75390535 | 15:91,503,195 | C/T | — | benign |
| rs2037289037 | 15:91,503,586 | G/C | — | uncertain significance |
| rs964561311 | 15:91,503,599 | G/A | — | uncertain significance |
| rs545375745 | 15:91,503,714 | C/T | — | uncertain significance |
| rs771592562 | 15:91,504,880 | A/G | — | uncertain significance |
| rs77876906 | 15:91,504,900 | C/T | — | benign |
| rs531863066 | 15:91,504,934 | G/A | — | uncertain significance |
| rs1456402226 | 15:91,504,939 | G/T | — | uncertain significance |
| rs181563086 | 15:91,504,944 | T/A | — | uncertain significance |
| rs145370091 | 15:91,504,953 | G/C | — | uncertain significance |
| rs549907340 | 15:91,504,970 | G/A | — | uncertain significance |
| rs8028409 | 15:91,506,422 | A/C | — | — |
| rs8037137 | 15:91,506,637 | T/C | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.