FAM184A
family with sequence similarity 184 member A
Summary
Located in several cellular components, including P-body; cytosol; and microtubule organizing center. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs773652152 | 6:119,281,285 | G/A | — | uncertain significance |
| rs763483819 | 6:119,281,295 | C/G | — | uncertain significance |
| rs548892238 | 6:119,281,333 | C/T | — | uncertain significance |
| rs764735318 | 6:119,283,028 | C/T | — | uncertain significance |
| rs759460715 | 6:119,283,073 | A/C | — | uncertain significance |
| rs780660408 | 6:119,283,123 | C/G | — | uncertain significance |
| rs371789193 | 6:119,288,009 | C/A | — | uncertain significance |
| rs200483949 | 6:119,288,065 | T/C | — | uncertain significance |
| rs762315481 | 6:119,295,660 | T/C | — | uncertain significance |
| rs766178587 | 6:119,295,705 | T/C | — | uncertain significance |
| rs1000905754 | 6:119,297,105 | T/G | — | uncertain significance |
| rs1783831114 | 6:119,297,113 | A/G | — | uncertain significance |
| rs749833051 | 6:119,297,120 | T/G | — | uncertain significance |
| rs2534880097 | 6:119,300,610 | A/G | — | uncertain significance |
| rs755407520 | 6:119,301,332 | T/C | — | uncertain significance |
| rs748796326 | 6:119,301,364 | A/G | — | uncertain significance |
| rs772006645 | 6:119,301,372 | G/T | — | uncertain significance |
| rs762127549 | 6:119,301,407 | G/T | — | uncertain significance |
| rs763081894 | 6:119,301,418 | A/G | — | uncertain significance |
| rs184403302 | 6:119,301,422 | G/A | — | uncertain significance |
| rs372303662 | 6:119,301,436 | G/A | — | uncertain significance |
| rs1412695582 | 6:119,301,449 | G/C | — | uncertain significance |
| rs200307028 | 6:119,301,460 | A/C | — | uncertain significance |
| rs772096482 | 6:119,301,496 | T/C | — | uncertain significance |
| rs952014895 | 6:119,324,143 | T/A | — | uncertain significance |
| rs759627751 | 6:119,324,155 | G/A | — | uncertain significance |
| rs369569160 | 6:119,324,756 | T/C | — | uncertain significance |
| rs371465166 | 6:119,327,706 | G/A | — | uncertain significance |
| rs2534957957 | 6:119,327,763 | A/G | — | uncertain significance |
| rs377057105 | 6:119,332,509 | C/T | — | uncertain significance |
| rs200578559 | 6:119,332,544 | T/C | — | uncertain significance |
| rs760594623 | 6:119,332,590 | C/T | — | uncertain significance |
| rs756769671 | 6:119,332,596 | C/G | — | uncertain significance |
| rs200619083 | 6:119,337,934 | C/G | — | uncertain significance |
| rs199729339 | 6:119,337,942 | A/T | — | uncertain significance |
| rs2534988097 | 6:119,337,977 | T/C | — | uncertain significance |
| rs368962680 | 6:119,341,187 | T/G | — | uncertain significance |
| rs1352733115 | 6:119,341,263 | T/G | — | uncertain significance |
| rs775837445 | 6:119,341,318 | A/G | — | uncertain significance |
| rs373985994 | 6:119,344,148 | C/T | — | uncertain significance |
| rs2535008428 | 6:119,344,155 | T/C | — | uncertain significance |
| rs376729872 | 6:119,344,245 | C/T | — | uncertain significance |
| rs12664251 | 6:119,344,546 | A/T | — | — |
| rs2114690397 | 6:119,345,143 | A/G | — | likely benign |
| rs777929359 | 6:119,345,155 | G/A | — | uncertain significance |
| rs2535012866 | 6:119,345,177 | C/T | — | uncertain significance |
| rs1785546955 | 6:119,345,209 | T/C | — | uncertain significance |
| rs778669337 | 6:119,345,356 | C/T | — | likely benign |
| rs1286024598 | 6:119,345,482 | G/C | — | uncertain significance |
| rs772609868 | 6:119,345,561 | C/A | — | uncertain significance |
| rs1269682715 | 6:119,345,609 | C/G | — | uncertain significance |
| rs564860341 | 6:119,345,629 | C/T | — | uncertain significance |
| rs753994706 | 6:119,345,630 | G/A | — | uncertain significance |
| rs112757909 | 6:119,345,687 | T/A | — | uncertain significance |
| rs765385387 | 6:119,345,920 | T/C | — | uncertain significance |
| rs750667265 | 6:119,345,933 | T/C | — | uncertain significance |
| rs200433019 | 6:119,399,333 | C/T | — | uncertain significance |
| rs201604238 | 6:119,399,349 | T/C | — | uncertain significance |
| rs370600021 | 6:119,399,351 | C/T | — | likely benign |
| rs976751055 | 6:119,399,370 | T/C | — | uncertain significance |
| rs1472915470 | 6:119,399,403 | G/A | — | uncertain significance |
| rs777174299 | 6:119,399,418 | G/A | — | uncertain significance |
| rs9489587 | 6:119,402,455 | C/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.