PARPBP
PARP1 binding protein
Summary
Predicted to enable DNA binding activity. Involved in negative regulation of double-strand break repair via homologous recombination. Located in chromatin and nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants45 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2292303 | 12:102,513,531 | G/C | regulatory region variant | — |
| rs370200754 | 12:102,517,761 | G/A | — | uncertain significance |
| rs528660652 | 12:102,517,784 | G/T | — | uncertain significance |
| rs768649483 | 12:102,517,803 | C/T | — | uncertain significance |
| rs368746845 | 12:102,540,754 | G/A | — | — |
| rs76825149 | 12:102,541,667 | A/G | intron variant | — |
| rs759270887 | 12:102,542,116 | T/A | — | uncertain significance |
| rs1885707493 | 12:102,542,126 | T/C | — | uncertain significance |
| rs755278471 | 12:102,542,165 | T/C | — | uncertain significance |
| rs143799695 | 12:102,542,181 | T/C | — | likely benign |
| rs148169413 | 12:102,542,188 | C/A | — | likely benign |
| rs140043679 | 12:102,542,200 | G/T | — | uncertain significance |
| rs113701417 | 12:102,551,715 | G/T | — | — |
| rs1004819261 | 12:102,558,288 | G/A | — | uncertain significance |
| rs760005249 | 12:102,558,303 | A/G | — | uncertain significance |
| rs1887931316 | 12:102,558,312 | G/A | — | uncertain significance |
| rs2502951315 | 12:102,558,371 | A/C | — | uncertain significance |
| rs772932575 | 12:102,559,531 | A/G | — | uncertain significance |
| rs747600346 | 12:102,559,631 | A/G | — | uncertain significance |
| rs989998438 | 12:102,559,632 | T/A | — | uncertain significance |
| rs1888089516 | 12:102,559,652 | C/A | — | uncertain significance |
| rs144580828 | 12:102,559,660 | A/C | — | uncertain significance |
| rs12424451 | 12:102,566,908 | A/G | intron variant | — |
| rs17438571 | 12:102,568,101 | A/G | regulatory region variant | — |
| rs775534662 | 12:102,569,263 | T/C | — | uncertain significance |
| rs2503406939 | 12:102,569,293 | A/G | — | uncertain significance |
| rs1233529208 | 12:102,569,296 | T/A | — | uncertain significance |
| rs147086486 | 12:102,569,436 | C/G | — | uncertain significance |
| rs76157805 | 12:102,571,933 | A/G | intron variant | — |
| rs764402553 | 12:102,572,406 | T/C | — | uncertain significance |
| rs11111197 | 12:102,579,519 | C/T | intron variant | — |
| rs17032311 | 12:102,587,534 | A/G | downstream gene variant | — |
| rs1363077047 | 12:102,589,126 | A/G | — | uncertain significance |
| rs1891205006 | 12:102,589,190 | C/T | — | uncertain significance |
| rs370128473 | 12:102,589,201 | C/G | — | uncertain significance |
| rs1891206999 | 12:102,589,207 | A/G | — | uncertain significance |
| rs750737952 | 12:102,589,768 | C/T | — | uncertain significance |
| rs534675334 | 12:102,589,805 | T/A | — | uncertain significance |
| rs759599506 | 12:102,589,822 | A/G | — | uncertain significance |
| rs141979957 | 12:102,589,900 | A/G | — | uncertain significance |
| rs1243853422 | 12:102,589,911 | C/T | — | uncertain significance |
| rs994772118 | 12:102,589,937 | A/G | — | uncertain significance |
| rs202184661 | 12:102,589,992 | G/A | — | uncertain significance |
| rs1396165735 | 12:102,590,025 | T/G | — | uncertain significance |
| rs763051485 | 12:102,590,050 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.