PWP2
PWP2 small subunit processome component
Summary
Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Part of small-subunit processome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773881408 | 21:45,528,876 | G/C | — | uncertain significance |
| rs758422082 | 21:45,528,896 | G/A | — | uncertain significance |
| rs776747279 | 21:45,528,920 | A/G | — | uncertain significance |
| rs754620881 | 21:45,528,961 | G/C | — | uncertain significance |
| rs145480446 | 21:45,529,016 | A/G | downstream gene variant | — |
| rs2039230791 | 21:45,533,654 | C/T | — | uncertain significance |
| rs367768618 | 21:45,533,666 | G/A | — | uncertain significance |
| rs139657835 | 21:45,533,696 | C/T | — | uncertain significance |
| rs58851899 | 21:45,533,720 | T/C | — | uncertain significance |
| rs151259638 | 21:45,534,069 | C/T | — | uncertain significance |
| rs778347598 | 21:45,534,084 | T/C | — | uncertain significance |
| rs146998876 | 21:45,534,087 | T/C | — | uncertain significance |
| rs545213060 | 21:45,534,126 | C/T | — | uncertain significance |
| rs1601871456 | 21:45,534,531 | A/C | — | uncertain significance |
| rs895830634 | 21:45,534,550 | C/T | — | uncertain significance |
| rs146014938 | 21:45,534,552 | C/T | — | uncertain significance |
| rs751020185 | 21:45,534,576 | G/C | — | uncertain significance |
| rs146454881 | 21:45,535,239 | G/A | — | uncertain significance |
| rs144385075 | 21:45,535,605 | A/C | — | uncertain significance |
| rs2517780387 | 21:45,535,675 | T/C | — | uncertain significance |
| rs372548179 | 21:45,535,719 | G/A | — | uncertain significance |
| rs1469475700 | 21:45,535,735 | T/A | — | uncertain significance |
| rs758855514 | 21:45,535,753 | C/T | — | uncertain significance |
| rs747552429 | 21:45,535,758 | G/A | — | uncertain significance |
| rs775706445 | 21:45,537,712 | A/G | — | uncertain significance |
| rs142364001 | 21:45,537,734 | C/A | — | uncertain significance |
| rs534731637 | 21:45,537,820 | A/C | — | uncertain significance |
| rs908874896 | 21:45,538,654 | C/A | — | uncertain significance |
| rs2517781291 | 21:45,538,661 | T/C | — | uncertain significance |
| rs574646908 | 21:45,539,319 | A/G | — | uncertain significance |
| rs144390937 | 21:45,539,378 | A/C | — | uncertain significance |
| rs145342801 | 21:45,540,275 | C/T | — | uncertain significance |
| rs2517781965 | 21:45,540,278 | A/G | — | uncertain significance |
| rs758980217 | 21:45,540,301 | G/T | — | uncertain significance |
| rs776850235 | 21:45,540,349 | G/A | — | uncertain significance |
| rs148867930 | 21:45,540,353 | C/G | — | uncertain significance |
| rs1357565921 | 21:45,540,544 | G/A | — | uncertain significance |
| rs749357091 | 21:45,540,591 | G/A | — | uncertain significance |
| rs144602866 | 21:45,540,609 | G/A | — | uncertain significance |
| rs750219783 | 21:45,540,636 | A/C | — | uncertain significance |
| rs2517782209 | 21:45,540,897 | C/T | — | uncertain significance |
| rs201712401 | 21:45,540,915 | A/G | — | likely benign |
| rs142281336 | 21:45,542,177 | G/A | — | uncertain significance |
| rs372545607 | 21:45,542,214 | C/T | — | uncertain significance |
| rs201036661 | 21:45,542,226 | C/T | — | uncertain significance |
| rs749414558 | 21:45,544,528 | G/A | — | uncertain significance |
| rs1041864351 | 21:45,544,543 | G/A | — | uncertain significance |
| rs773541437 | 21:45,544,546 | C/T | — | uncertain significance |
| rs752404039 | 21:45,544,558 | C/G | — | uncertain significance |
| rs146698767 | 21:45,544,573 | G/A | — | uncertain significance |
| rs753733213 | 21:45,545,943 | G/C | — | uncertain significance |
| rs200027667 | 21:45,545,991 | G/A | — | uncertain significance |
| rs757857003 | 21:45,546,832 | G/A | — | uncertain significance |
| rs373315890 | 21:45,547,816 | G/A | — | uncertain significance |
| rs144002518 | 21:45,547,837 | C/T | — | uncertain significance |
| rs370806722 | 21:45,547,869 | C/T | — | uncertain significance |
| rs1026488769 | 21:45,547,908 | A/G | — | uncertain significance |
| rs144699601 | 21:45,547,912 | C/T | — | uncertain significance |
| rs777992855 | 21:45,547,914 | G/C | — | uncertain significance |
| rs923387270 | 21:45,547,929 | G/A | — | uncertain significance |
| rs754703859 | 21:45,547,935 | C/T | — | uncertain significance |
| rs2517783948 | 21:45,548,001 | G/C | — | uncertain significance |
| rs1569244740 | 21:45,548,133 | G/A | — | uncertain significance |
| rs745909244 | 21:45,548,224 | A/G | — | uncertain significance |
| rs1403438147 | 21:45,548,240 | C/A | — | likely benign |
| rs2517784054 | 21:45,548,250 | A/T | — | uncertain significance |
| rs145366629 | 21:45,548,460 | G/T | — | uncertain significance |
| rs148288077 | 21:45,550,499 | A/C | — | uncertain significance |
| rs202042327 | 21:45,550,504 | C/G | — | uncertain significance |
| rs773875876 | 21:45,550,570 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.