ARMC12
armadillo repeat containing 12
Summary
Involved in positive regulation of cell growth and sperm mitochondrial sheath assembly. Located in nucleus. Implicated in spermatogenic failure 90. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs143012564 | 6:35,704,928 | C/T | — | uncertain significance |
| rs755088430 | 6:35,704,937 | G/A | — | uncertain significance |
| rs769372787 | 6:35,705,067 | G/C | — | uncertain significance |
| rs386352286 | 6:35,705,076 | C/T | — | uncertain significance |
| rs1020056210 | 6:35,705,086 | G/C | — | uncertain significance |
| rs138730820 | 6:35,705,825 | G/A | — | uncertain significance |
| rs202136403 | 6:35,705,834 | G/A | — | uncertain significance |
| rs151133317 | 6:35,705,853 | G/A | — | likely benign |
| rs756110834 | 6:35,706,162 | C/T | — | uncertain significance |
| rs142208066 | 6:35,706,177 | C/T | — | uncertain significance |
| rs768837601 | 6:35,706,197 | G/A | — | uncertain significance |
| rs145912136 | 6:35,706,235 | C/T | synonymous variant | — |
| rs551634156 | 6:35,707,559 | C/T | — | — |
| rs79354046 | 6:35,713,835 | A/T | intron variant | — |
| rs144687290 | 6:35,715,051 | A/T | — | uncertain significance |
| rs148096096 | 6:35,715,059 | G/A | — | uncertain significance |
| rs753132304 | 6:35,715,135 | A/G | — | uncertain significance |
| rs193921111 | 6:35,715,194 | G/T | — | uncertain significance |
| rs200319789 | 6:35,715,366 | G/A | — | pathogenic |
| rs776728534 | 6:35,715,369 | T/C | — | pathogenic |
| rs200749169 | 6:35,715,420 | G/A | — | pathogenic |
| rs373958570 | 6:35,716,408 | C/T | — | uncertain significance |
| rs745634515 | 6:35,716,487 | C/T | — | uncertain significance |
| rs762538474 | 6:35,716,562 | T/C | — | uncertain significance |
| rs187241615 | 6:35,716,618 | A/G | — | uncertain significance |
| rs377035170 | 6:35,716,640 | C/T | — | uncertain significance |
| rs2766547 | 6:35,717,043 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.