FHIP2B
FHF complex subunit HOOK interacting protein 2B
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1319202578 | 8:21,946,780 | G/C | — | uncertain significance |
| rs575168429 | 8:21,946,804 | G/C | — | uncertain significance |
| rs369091522 | 8:21,952,010 | C/G | — | uncertain significance |
| rs765792078 | 8:21,953,859 | C/T | — | uncertain significance |
| rs1323170128 | 8:21,953,917 | A/G | — | uncertain significance |
| rs566229900 | 8:21,953,944 | G/A | — | uncertain significance |
| rs773503897 | 8:21,954,004 | C/T | — | uncertain significance |
| rs201073655 | 8:21,954,018 | G/A | — | uncertain significance |
| rs374147568 | 8:21,955,036 | G/A | — | uncertain significance |
| rs747529832 | 8:21,955,258 | G/A | — | uncertain significance |
| rs745726476 | 8:21,955,295 | C/T | — | uncertain significance |
| rs775211664 | 8:21,955,297 | G/A | — | uncertain significance |
| rs776813466 | 8:21,955,316 | A/G | — | uncertain significance |
| rs751932847 | 8:21,955,336 | G/A | — | likely benign |
| rs199544823 | 8:21,955,598 | G/C | — | uncertain significance |
| rs370489747 | 8:21,955,678 | G/A | — | uncertain significance |
| rs139434422 | 8:21,955,765 | G/T | — | uncertain significance |
| rs1175667820 | 8:21,955,810 | T/A | — | uncertain significance |
| rs536224294 | 8:21,956,070 | G/A | — | likely benign |
| rs1158663856 | 8:21,956,479 | A/C | — | uncertain significance |
| rs746792316 | 8:21,956,856 | C/T | — | uncertain significance |
| rs371554448 | 8:21,956,869 | C/A | — | uncertain significance |
| rs376572772 | 8:21,956,870 | G/A | — | uncertain significance |
| rs377050503 | 8:21,957,264 | C/T | — | uncertain significance |
| rs200510567 | 8:21,957,274 | G/A | — | uncertain significance |
| rs760542223 | 8:21,957,283 | C/T | — | uncertain significance |
| rs535908714 | 8:21,957,292 | G/A | — | likely benign |
| rs371010422 | 8:21,957,339 | C/T | — | uncertain significance |
| rs758473616 | 8:21,957,378 | G/A | — | likely benign |
| rs367649297 | 8:21,957,379 | G/A | — | uncertain significance |
| rs2538823082 | 8:21,957,390 | C/T | — | uncertain significance |
| rs200398281 | 8:21,957,391 | A/G | — | uncertain significance |
| rs772947373 | 8:21,958,114 | A/G | — | likely benign |
| rs780038200 | 8:21,958,375 | A/G | — | uncertain significance |
| rs753314687 | 8:21,958,422 | C/T | — | uncertain significance |
| rs369364643 | 8:21,958,953 | T/A | — | uncertain significance |
| rs775394872 | 8:21,958,954 | C/G | — | uncertain significance |
| rs747585450 | 8:21,959,027 | G/A | — | uncertain significance |
| rs780495400 | 8:21,959,237 | C/T | — | uncertain significance |
| rs752025525 | 8:21,959,238 | G/T | — | uncertain significance |
| rs376452168 | 8:21,959,240 | G/A | — | uncertain significance |
| rs1269931842 | 8:21,959,243 | G/A | — | uncertain significance |
| rs2538834067 | 8:21,959,316 | A/G | — | uncertain significance |
| rs778662130 | 8:21,959,325 | G/A | — | likely benign |
| rs200291135 | 8:21,959,333 | T/C | — | uncertain significance |
| rs769595796 | 8:21,959,343 | T/A | — | uncertain significance |
| rs113817175 | 8:21,959,726 | G/A | — | likely benign |
| rs752175859 | 8:21,959,794 | G/A | — | uncertain significance |
| rs763795141 | 8:21,960,048 | G/C | — | uncertain significance |
| rs549339194 | 8:21,960,066 | C/G | — | uncertain significance |
| rs751464696 | 8:21,960,097 | T/G | — | uncertain significance |
| rs750775564 | 8:21,960,105 | C/T | — | uncertain significance |
| rs375585613 | 8:21,960,332 | G/A | — | uncertain significance |
| rs201855595 | 8:21,960,359 | G/A | — | uncertain significance |
| rs769305209 | 8:21,960,393 | C/A | — | uncertain significance |
| rs371562419 | 8:21,960,413 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.