DMAC2
distal membrane arm assembly component 2
Summary
Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants33 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17318596 | 19:41,937,095 | G/A | regulatory region variant | — |
| rs782554050 | 19:41,938,147 | C/T | — | likely benign |
| rs2231945 | 19:41,938,164 | C/T | — | likely benign |
| rs2513472337 | 19:41,938,191 | A/G | — | uncertain significance |
| rs1555769169 | 19:41,938,201 | C/T | — | uncertain significance |
| rs2513472578 | 19:41,938,218 | A/G | — | uncertain significance |
| rs2231943 | 19:41,938,222 | T/C | — | not provided |
| rs201804717 | 19:41,938,223 | G/A | — | likely benign |
| rs782212578 | 19:41,938,226 | A/T | — | uncertain significance |
| rs201728769 | 19:41,938,227 | T/C | — | uncertain significance |
| rs143331885 | 19:41,938,289 | C/T | — | likely benign |
| rs149741041 | 19:41,938,295 | G/A | — | likely benign |
| rs782307590 | 19:41,938,309 | G/A | — | uncertain significance |
| rs67047091 | 19:41,938,684 | C/T | — | — |
| rs144637709 | 19:41,939,196 | C/T | — | uncertain significance |
| rs782057190 | 19:41,939,204 | C/T | — | uncertain significance |
| rs367830809 | 19:41,939,226 | C/T | — | uncertain significance |
| rs782413672 | 19:41,939,271 | G/A | — | uncertain significance |
| rs1043413 | 19:41,939,297 | C/G | missense variant | — |
| rs781938587 | 19:41,939,336 | C/T | — | uncertain significance |
| rs141059890 | 19:41,939,460 | C/T | — | uncertain significance |
| rs1343618242 | 19:41,939,463 | A/G | — | uncertain significance |
| rs145875700 | 19:41,939,502 | G/C | — | uncertain significance |
| rs148919104 | 19:41,939,543 | T/C | — | uncertain significance |
| rs1555771174 | 19:41,942,309 | C/T | — | uncertain significance |
| rs782625556 | 19:41,942,340 | C/T | — | likely benign |
| rs566734225 | 19:41,942,351 | T/C | — | uncertain significance |
| rs782651061 | 19:41,944,187 | C/T | — | uncertain significance |
| rs185885524 | 19:41,944,192 | A/T | — | uncertain significance |
| rs782664653 | 19:41,944,258 | G/A | — | uncertain significance |
| rs2231939 | 19:41,944,270 | T/C | — | likely benign |
| rs377191429 | 19:41,944,312 | C/T | — | likely benign |
| rs13346603 | 19:41,945,837 | T/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.