MAGEA3
MAGE family member A3
Summary
This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1179127435 | X:151,869,619 | T/T | — | likely benign |
| rs1248162986 | X:151,869,653 | A/A | — | likely benign |
| rs7057497 | X:151,869,745 | C/C | — | benign |
| rs782460836 | X:151,869,776 | G/G | — | likely benign |
| rs782764980 | X:151,869,777 | A/A | — | likely benign |
| rs1556826649 | X:151,869,922 | C/T | — | benign |
| rs1216061789 | X:151,870,114 | C/C | — | benign |
| rs1556827155 | X:151,870,189 | C/T | — | benign |
| rs1290943393 | X:151,870,233 | C/C | — | benign |
| rs782339504 | X:151,870,237 | G/T | — | benign |
| rs1556827244 | X:151,935,234 | C/A | — | uncertain significance |
| rs1931778312 | X:151,935,266 | A/G | — | uncertain significance |
| rs1556827180 | X:151,935,272 | T/C | — | uncertain significance |
| rs1556827170 | X:151,935,275 | G/T | — | uncertain significance |
| rs1421845987 | X:151,935,278 | G/C | — | uncertain significance |
| rs149795670 | X:151,935,287 | T/C | — | uncertain significance |
| rs1361909824 | X:151,935,332 | C/T | — | uncertain significance |
| rs1556826927 | X:151,935,407 | T/C | — | uncertain significance |
| rs2521489922 | X:151,935,442 | G/A | — | uncertain significance |
| rs149483923 | X:151,935,470 | C/T | — | uncertain significance |
| rs141132459 | X:151,935,540 | G/A | — | likely benign |
| rs782412538 | X:151,935,646 | T/C | — | uncertain significance |
| rs7056365 | X:151,935,712 | C/G | missense variant | — |
| rs782278365 | X:151,935,749 | C/T | — | uncertain significance |
| rs140660790 | X:151,935,793 | C/T | — | uncertain significance |
| rs2521483198 | X:151,935,818 | C/T | — | uncertain significance |
| rs2124945229 | X:151,935,831 | C/G | — | uncertain significance |
| rs782483422 | X:151,935,838 | C/T | — | uncertain significance |
| rs1931736743 | X:151,935,856 | T/C | — | likely benign |
| rs1931730670 | X:151,935,961 | G/T | — | uncertain significance |
| rs1931723321 | X:151,936,067 | C/G | — | uncertain significance |
| rs782605651 | X:151,936,084 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.