FAM120B
family with sequence similarity 120 member B
Summary
Predicted to be involved in fat cell differentiation and peroxisome proliferator activated receptor signaling pathway. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62425620 | 6:170,605,956 | C/T | regulatory region variant | — |
| rs4995139 | 6:170,607,609 | T/A | — | — |
| rs9460106 | 6:170,615,960 | T/C | regulatory region variant | — |
| rs75799561 | 6:170,616,248 | A/C | regulatory region variant | — |
| rs2483459483 | 6:170,626,516 | C/T | — | uncertain significance |
| rs1418294738 | 6:170,626,579 | A/T | — | uncertain significance |
| rs372574876 | 6:170,626,615 | T/C | — | uncertain significance |
| rs2483461460 | 6:170,626,696 | A/G | — | uncertain significance |
| rs1479852978 | 6:170,626,755 | G/A | — | uncertain significance |
| rs780725538 | 6:170,626,953 | G/A | — | uncertain significance |
| rs769513162 | 6:170,626,965 | G/A | — | uncertain significance |
| rs1785003137 | 6:170,626,984 | A/G | — | uncertain significance |
| rs751590046 | 6:170,627,061 | G/A | — | uncertain significance |
| rs2483466772 | 6:170,627,122 | T/C | — | uncertain significance |
| rs142483267 | 6:170,627,175 | A/G | — | uncertain significance |
| rs767205522 | 6:170,627,238 | A/G | — | uncertain significance |
| rs1480413905 | 6:170,627,297 | A/C | — | uncertain significance |
| rs200854692 | 6:170,627,437 | G/A | — | uncertain significance |
| rs146980569 | 6:170,627,481 | G/A | — | uncertain significance |
| rs1316867114 | 6:170,627,484 | G/A | — | uncertain significance |
| rs995191901 | 6:170,627,545 | G/T | — | uncertain significance |
| rs6917485 | 6:170,627,586 | G/A | — | uncertain significance |
| rs1400681571 | 6:170,627,589 | T/C | — | likely benign |
| rs201677849 | 6:170,627,631 | C/T | — | likely benign |
| rs148592361 | 6:170,627,687 | G/A | — | uncertain significance |
| rs200811562 | 6:170,627,737 | A/T | — | uncertain significance |
| rs775919338 | 6:170,627,758 | T/C | — | uncertain significance |
| rs879126817 | 6:170,627,805 | T/C | — | likely benign |
| rs887776669 | 6:170,627,835 | A/G | — | uncertain significance |
| rs137909655 | 6:170,627,842 | C/T | — | uncertain significance |
| rs2483478618 | 6:170,627,848 | C/A | — | uncertain significance |
| rs141508700 | 6:170,627,983 | A/G | — | uncertain significance |
| rs376805450 | 6:170,628,004 | C/T | — | uncertain significance |
| rs764129722 | 6:170,628,008 | A/G | — | likely benign |
| rs766907261 | 6:170,628,015 | G/C | — | uncertain significance |
| rs2483481255 | 6:170,628,022 | T/C | — | uncertain significance |
| rs1785120401 | 6:170,628,105 | G/C | — | uncertain significance |
| rs895164979 | 6:170,628,165 | G/A | — | uncertain significance |
| rs200658999 | 6:170,632,242 | A/G | — | uncertain significance |
| rs749518462 | 6:170,632,286 | G/C | — | uncertain significance |
| rs773629402 | 6:170,639,555 | T/C | — | likely benign |
| rs766744846 | 6:170,639,564 | A/C | — | uncertain significance |
| rs201594993 | 6:170,657,361 | G/A | — | uncertain significance |
| rs147192106 | 6:170,662,284 | G/A | intron variant | — |
| rs2103816 | 6:170,676,013 | T/A | regulatory region variant | — |
| rs1790312508 | 6:170,697,483 | G/C | — | uncertain significance |
| rs972999325 | 6:170,697,570 | T/G | — | likely benign |
| rs775268728 | 6:170,700,108 | G/A | — | uncertain significance |
| rs138440511 | 6:170,700,170 | C/T | — | uncertain significance |
| rs2483424342 | 6:170,704,579 | G/C | — | uncertain significance |
| rs773813812 | 6:170,704,587 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.