AFM
afamin
Summary
This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream. [provided by RefSeq, Jul 2008]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs531634253 | 4:74,347,571 | C/T | — | uncertain significance |
| rs139818614 | 4:74,348,586 | G/A | intron variant | — |
| rs1894292 | 4:74,349,158 | G/A | intron variant | — |
| rs752012336 | 4:74,349,668 | T/G | — | uncertain significance |
| rs781727350 | 4:74,349,675 | C/A | — | uncertain significance |
| rs768090251 | 4:74,350,009 | G/C | — | uncertain significance |
| rs1253978636 | 4:74,350,042 | G/T | — | uncertain significance |
| rs757913302 | 4:74,350,075 | G/A | — | uncertain significance |
| rs777617182 | 4:74,350,082 | C/T | — | uncertain significance |
| rs1218198401 | 4:74,350,094 | G/T | — | uncertain significance |
| rs1225829118 | 4:74,351,658 | T/A | — | uncertain significance |
| rs146636018 | 4:74,351,717 | C/T | — | uncertain significance |
| rs375914166 | 4:74,351,756 | G/C | — | uncertain significance |
| rs72856634 | 4:74,352,631 | C/T | intron variant | — |
| rs2476242622 | 4:74,352,711 | C/A | — | uncertain significance |
| rs2476242725 | 4:74,352,742 | G/A | — | uncertain significance |
| rs61747694 | 4:74,352,800 | A/C | — | uncertain significance |
| rs765287577 | 4:74,353,457 | A/G | — | uncertain significance |
| rs754533350 | 4:74,354,355 | C/T | — | uncertain significance |
| rs139224995 | 4:74,354,406 | T/C | — | uncertain significance |
| rs144025350 | 4:74,354,432 | G/T | — | uncertain significance |
| rs368606268 | 4:74,354,468 | C/T | — | uncertain significance |
| rs867565889 | 4:74,357,737 | G/A | — | uncertain significance |
| rs2476252174 | 4:74,357,744 | T/A | — | uncertain significance |
| rs758690639 | 4:74,357,752 | G/A | — | uncertain significance |
| rs1274074014 | 4:74,357,766 | C/G | — | likely benign |
| rs151113361 | 4:74,357,800 | C/A | — | uncertain significance |
| rs72856641 | 4:74,359,582 | T/C | intron variant | — |
| rs759368825 | 4:74,361,026 | T/G | — | uncertain significance |
| rs146713717 | 4:74,361,028 | A/G | — | uncertain significance |
| rs200798387 | 4:74,361,036 | A/G | — | uncertain significance |
| rs777577891 | 4:74,361,075 | A/G | — | uncertain significance |
| rs372542885 | 4:74,361,147 | G/A | — | uncertain significance |
| rs1467591885 | 4:74,363,385 | A/G | — | uncertain significance |
| rs754857165 | 4:74,364,843 | G/C | — | uncertain significance |
| rs2476263031 | 4:74,364,856 | G/C | — | uncertain significance |
| rs769742032 | 4:74,364,895 | G/A | — | likely benign |
| rs1721345413 | 4:74,364,904 | G/T | — | uncertain significance |
| rs199782653 | 4:74,364,946 | G/A | — | uncertain significance |
| rs2476264500 | 4:74,365,731 | T/G | — | uncertain significance |
| rs761697468 | 4:74,365,775 | C/T | — | uncertain significance |
| rs767460010 | 4:74,365,776 | C/G | — | uncertain significance |
| rs752104326 | 4:74,365,836 | T/G | — | uncertain significance |
| rs777843991 | 4:74,367,515 | A/T | — | uncertain significance |
| rs768706430 | 4:74,367,546 | T/G | — | uncertain significance |
| rs757078588 | 4:74,367,595 | T/G | — | uncertain significance |
| rs1308025899 | 4:74,368,780 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.