MXRA7
matrix remodeling associated 7
Summary
Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs202238128 | 17:74,673,686 | C/T | — | uncertain significance |
| rs2076251670 | 17:74,673,735 | T/C | — | uncertain significance |
| rs773478863 | 17:74,673,767 | A/G | — | uncertain significance |
| rs751375441 | 17:74,673,783 | C/T | — | uncertain significance |
| rs111262383 | 17:74,675,667 | A/C | intron variant | — |
| rs770620809 | 17:74,681,164 | C/T | — | uncertain significance |
| rs144263669 | 17:74,681,190 | T/A | — | uncertain significance |
| rs780809283 | 17:74,681,244 | T/C | — | uncertain significance |
| rs720782 | 17:74,682,602 | C/T | intron variant | — |
| rs2286589 | 17:74,684,080 | G/A | intron variant | — |
| rs142545326 | 17:74,684,196 | G/T | — | uncertain significance |
| rs994854079 | 17:74,684,199 | C/G | — | likely benign |
| rs188871607 | 17:74,684,439 | G/A | — | likely benign |
| rs7219390 | 17:74,684,858 | T/C | regulatory region variant | — |
| rs35504735 | 17:74,686,809 | A/G | intron variant | — |
| rs75118211 | 17:74,700,311 | G/A | upstream gene variant | — |
| rs4789349 | 17:74,706,341 | A/G | — | — |
| rs71383083 | 17:74,706,346 | G/C | — | — |
| rs539341681 | 17:74,706,706 | T/A | — | uncertain significance |
| rs762048171 | 17:74,706,710 | C/T | — | uncertain significance |
| rs2509668956 | 17:74,706,725 | G/T | — | uncertain significance |
| rs1432152768 | 17:74,706,797 | C/A | — | uncertain significance |
| rs1040801249 | 17:74,706,893 | G/A | — | uncertain significance |
| rs751463433 | 17:74,706,946 | C/T | missense variant | — |
| rs2076715789 | 17:74,707,018 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.