RAVER1
ribonucleoprotein, PTB binding 1
Summary
Enables RNA binding activity. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs867065326 | 19:10,428,134 | A/G | — | uncertain significance |
| rs780496917 | 19:10,428,406 | C/T | — | uncertain significance |
| rs377043925 | 19:10,428,422 | C/T | — | uncertain significance |
| rs1462720167 | 19:10,429,031 | A/T | — | uncertain significance |
| rs111808396 | 19:10,429,740 | A/G | upstream gene variant | — |
| rs1208080135 | 19:10,429,846 | T/C | — | uncertain significance |
| rs374391089 | 19:10,429,849 | C/A | — | uncertain significance |
| rs780876679 | 19:10,429,882 | C/T | — | uncertain significance |
| rs769028832 | 19:10,429,904 | G/A | — | uncertain significance |
| rs281426 | 19:10,431,051 | G/A | upstream gene variant | — |
| rs368092939 | 19:10,431,342 | C/T | — | uncertain significance |
| rs753739331 | 19:10,431,383 | C/T | — | uncertain significance |
| rs749663791 | 19:10,431,507 | C/T | — | uncertain significance |
| rs775046616 | 19:10,431,782 | C/T | — | uncertain significance |
| rs281425 | 19:10,431,799 | G/T | — | benign |
| rs2512389393 | 19:10,431,803 | G/T | — | uncertain significance |
| rs1351428370 | 19:10,431,905 | C/T | — | uncertain significance |
| rs1039208917 | 19:10,431,908 | G/C | — | uncertain significance |
| rs553388484 | 19:10,431,920 | G/A | — | uncertain significance |
| rs574742453 | 19:10,431,924 | G/A | — | uncertain significance |
| rs111778915 | 19:10,432,288 | C/T | — | uncertain significance |
| rs140231926 | 19:10,432,989 | T/C | upstream gene variant | — |
| rs898956236 | 19:10,433,325 | T/C | — | uncertain significance |
| rs373855534 | 19:10,433,337 | T/C | — | uncertain significance |
| rs540122915 | 19:10,433,388 | G/A | — | uncertain significance |
| rs199738113 | 19:10,433,832 | C/A | — | uncertain significance |
| rs372169479 | 19:10,433,835 | G/A | — | uncertain significance |
| rs368847000 | 19:10,433,878 | C/T | — | uncertain significance |
| rs201280904 | 19:10,433,913 | T/C | — | uncertain significance |
| rs774395999 | 19:10,433,940 | C/T | — | uncertain significance |
| rs767186725 | 19:10,434,205 | G/A | — | uncertain significance |
| rs12611016 | 19:10,434,886 | G/A | upstream gene variant | — |
| rs752870032 | 19:10,439,356 | G/A | — | uncertain significance |
| rs562246379 | 19:10,439,374 | C/T | — | uncertain significance |
| rs764354352 | 19:10,439,451 | G/A | — | uncertain significance |
| rs780779554 | 19:10,439,499 | T/G | — | uncertain significance |
| rs2512397524 | 19:10,439,578 | T/C | — | uncertain significance |
| rs1280748861 | 19:10,439,625 | T/A | — | uncertain significance |
| rs751524914 | 19:10,439,650 | T/A | — | uncertain significance |
| rs1375300162 | 19:10,439,713 | G/A | — | uncertain significance |
| rs200295536 | 19:10,439,755 | C/T | — | uncertain significance |
| rs2512399033 | 19:10,441,138 | G/C | — | uncertain significance |
| rs281412 | 19:10,441,474 | T/C | downstream gene variant | — |
| rs1339360039 | 19:10,444,152 | G/A | — | uncertain significance |
| rs748751957 | 19:10,444,156 | G/A | — | uncertain significance |
| rs770370470 | 19:10,444,159 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.