FCRL6
Fc receptor like 6
Summary
Enables MHC class II protein binding activity and protein phosphatase binding activity. Predicted to be involved in cell surface receptor signaling pathway and immune response. Located in external side of plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs189750399 | 1:159,769,958 | A/C | upstream gene variant | — |
| rs148468513 | 1:159,771,469 | C/A | upstream gene variant | — |
| rs749590419 | 1:159,778,057 | T/C | — | uncertain significance |
| rs751053507 | 1:159,778,132 | G/C | — | uncertain significance |
| rs925142301 | 1:159,778,136 | C/T | — | uncertain significance |
| rs1339126736 | 1:159,778,138 | G/A | — | uncertain significance |
| rs147917646 | 1:159,778,148 | G/A | — | benign |
| rs2524832176 | 1:159,778,162 | T/G | — | uncertain significance |
| rs140069687 | 1:159,778,165 | T/A | — | likely benign |
| rs149327737 | 1:159,778,754 | T/A | — | uncertain significance |
| rs145922130 | 1:159,778,798 | C/T | stop gained | — |
| rs140295172 | 1:159,778,822 | A/G | — | uncertain significance |
| rs148571854 | 1:159,778,905 | C/T | — | benign |
| rs377697676 | 1:159,778,907 | G/A | — | uncertain significance |
| rs146427544 | 1:159,778,931 | T/G | — | uncertain significance |
| rs538641740 | 1:159,778,935 | G/A | — | likely benign |
| rs371203584 | 1:159,778,957 | G/T | — | uncertain significance |
| rs1326268018 | 1:159,778,975 | G/A | — | uncertain significance |
| rs769087449 | 1:159,779,044 | G/A | — | likely benign |
| rs77146676 | 1:159,779,204 | G/A | — | uncertain significance |
| rs749978321 | 1:159,779,219 | T/C | — | uncertain significance |
| rs139067829 | 1:159,779,227 | G/T | — | uncertain significance |
| rs774886413 | 1:159,779,249 | G/A | — | uncertain significance |
| rs760965841 | 1:159,779,255 | T/C | — | uncertain significance |
| rs779386992 | 1:159,779,288 | C/T | — | uncertain significance |
| rs149576319 | 1:159,779,371 | C/A | — | uncertain significance |
| rs762747220 | 1:159,779,372 | T/C | — | uncertain significance |
| rs138930155 | 1:159,779,390 | A/G | — | uncertain significance |
| rs143179337 | 1:159,779,426 | A/G | — | uncertain significance |
| rs115855950 | 1:159,779,464 | T/C | — | benign |
| rs200994996 | 1:159,779,971 | C/T | — | uncertain significance |
| rs779840841 | 1:159,780,004 | C/G | — | uncertain significance |
| rs6657365 | 1:159,782,549 | C/G | intron variant | — |
| rs78228389 | 1:159,783,225 | G/A | intron variant | — |
| rs1427900436 | 1:159,783,299 | C/T | — | uncertain significance |
| rs572864590 | 1:159,783,302 | C/T | — | uncertain significance |
| rs58240276 | 1:159,783,559 | C/T | intron variant | — |
| rs140546327 | 1:159,784,059 | A/G | — | uncertain significance |
| rs149948473 | 1:159,784,077 | G/A | — | uncertain significance |
| rs12083595 | 1:159,784,357 | A/G | intron variant | — |
| rs369284673 | 1:159,785,239 | T/C | — | likely benign |
| rs140105569 | 1:159,785,427 | C/T | — | benign |
| rs146779081 | 1:159,785,428 | G/A | — | uncertain significance |
| rs368925722 | 1:159,785,439 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.