USHBP1
USH1 protein network component harmonin binding protein 1
Summary
Enables PDZ domain binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants61 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs35686037 | 19:17,359,535 | C/T | regulatory region variant | — |
| rs529233430 | 19:17,361,053 | A/G | — | likely benign |
| rs199788991 | 19:17,361,063 | G/T | — | uncertain significance |
| rs776539877 | 19:17,361,065 | G/A | — | uncertain significance |
| rs537440882 | 19:17,361,089 | A/T | — | uncertain significance |
| rs756523964 | 19:17,361,108 | C/T | — | uncertain significance |
| rs772292775 | 19:17,361,185 | T/C | — | uncertain significance |
| rs147601359 | 19:17,361,203 | C/T | — | uncertain significance |
| rs143580327 | 19:17,361,223 | G/A | — | likely benign |
| rs148037291 | 19:17,362,404 | A/G | — | uncertain significance |
| rs781210059 | 19:17,362,422 | C/T | — | uncertain significance |
| rs764849437 | 19:17,362,445 | C/T | — | uncertain significance |
| rs2073558111 | 19:17,362,747 | G/A | — | uncertain significance |
| rs2513068542 | 19:17,366,225 | C/T | — | uncertain significance |
| rs371019077 | 19:17,366,233 | G/T | — | uncertain significance |
| rs745887827 | 19:17,366,277 | C/T | — | uncertain significance |
| rs375541213 | 19:17,366,282 | C/G | — | uncertain significance |
| rs749424514 | 19:17,366,333 | C/T | — | uncertain significance |
| rs375995208 | 19:17,366,349 | G/A | — | uncertain significance |
| rs148585131 | 19:17,366,373 | G/A | — | uncertain significance |
| rs751215867 | 19:17,366,379 | C/T | — | uncertain significance |
| rs2513070300 | 19:17,367,284 | G/T | — | uncertain significance |
| rs1243888229 | 19:17,367,326 | G/A | — | uncertain significance |
| rs755814839 | 19:17,367,375 | C/T | — | uncertain significance |
| rs376454461 | 19:17,367,417 | G/C | — | uncertain significance |
| rs184887926 | 19:17,367,459 | G/A | — | uncertain significance |
| rs377574461 | 19:17,369,154 | G/A | — | uncertain significance |
| rs2073658725 | 19:17,370,102 | A/G | — | uncertain significance |
| rs766379332 | 19:17,370,173 | C/A | — | uncertain significance |
| rs776386065 | 19:17,370,434 | G/C | — | uncertain significance |
| rs201874448 | 19:17,370,469 | G/A | — | uncertain significance |
| rs779238889 | 19:17,370,510 | C/T | — | uncertain significance |
| rs188069399 | 19:17,370,511 | G/A | — | uncertain significance |
| rs2513077935 | 19:17,370,528 | A/G | — | uncertain significance |
| rs148844083 | 19:17,370,777 | G/A | — | uncertain significance |
| rs12982178 | 19:17,371,568 | T/C | regulatory region variant | — |
| rs45520737 | 19:17,373,368 | T/C | — | uncertain significance |
| rs770082162 | 19:17,373,389 | C/T | — | likely benign |
| rs764919205 | 19:17,373,417 | G/A | — | uncertain significance |
| rs371303787 | 19:17,373,426 | C/T | — | uncertain significance |
| rs762798138 | 19:17,373,429 | C/G | — | uncertain significance |
| rs371750032 | 19:17,373,435 | G/C | — | uncertain significance |
| rs769029319 | 19:17,373,452 | C/T | — | uncertain significance |
| rs559894951 | 19:17,373,471 | C/T | — | uncertain significance |
| rs1404010501 | 19:17,373,501 | T/A | — | uncertain significance |
| rs140363005 | 19:17,373,504 | C/G | — | uncertain significance |
| rs149373392 | 19:17,373,594 | G/A | — | uncertain significance |
| rs765881807 | 19:17,373,608 | G/A | — | uncertain significance |
| rs746150934 | 19:17,373,635 | T/A | — | uncertain significance |
| rs1427337556 | 19:17,373,698 | G/T | — | uncertain significance |
| rs201280172 | 19:17,373,780 | C/T | — | uncertain significance |
| rs990704595 | 19:17,373,781 | A/T | — | uncertain significance |
| rs768501914 | 19:17,373,785 | A/G | — | likely benign |
| rs768002936 | 19:17,374,877 | G/A | — | uncertain significance |
| rs199639123 | 19:17,374,886 | G/A | — | likely benign |
| rs773882958 | 19:17,374,936 | C/G | — | uncertain significance |
| rs149022063 | 19:17,375,060 | G/C | — | uncertain significance |
| rs373645384 | 19:17,375,078 | G/A | — | uncertain significance |
| rs368129486 | 19:17,375,092 | G/A | — | uncertain significance |
| rs202066017 | 19:17,375,096 | C/T | — | uncertain significance |
| rs759387994 | 19:17,375,098 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.