ARMC2
armadillo repeat containing 2
Summary
Involved in sperm axoneme assembly. Implicated in spermatogenic failure 38. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs964353439 | 6:109,175,504 | C/G | — | uncertain significance |
| rs1774314987 | 6:109,175,555 | A/T | — | uncertain significance |
| rs147935937 | 6:109,175,625 | A/C | — | likely benign |
| rs374802762 | 6:109,175,684 | T/C | — | uncertain significance |
| rs116681118 | 6:109,179,398 | C/T | — | benign |
| rs2482734916 | 6:109,179,436 | A/G | — | uncertain significance |
| rs771178912 | 6:109,179,454 | C/T | — | uncertain significance |
| rs73524086 | 6:109,190,032 | G/A | — | benign |
| rs1776097078 | 6:109,190,055 | G/A | — | uncertain significance |
| rs199686045 | 6:109,190,094 | T/A | — | uncertain significance |
| rs372533595 | 6:109,190,103 | C/T | — | uncertain significance |
| rs144751024 | 6:109,190,140 | A/G | — | likely benign |
| rs1776106734 | 6:109,190,143 | C/T | — | likely benign |
| rs761127076 | 6:109,190,144 | A/G | — | uncertain significance |
| rs1373135059 | 6:109,190,145 | G/A | — | uncertain significance |
| rs1562332833 | 6:109,190,156 | C/T | — | pathogenic |
| rs539620053 | 6:109,190,172 | C/T | — | uncertain significance |
| rs9386758 | 6:109,197,379 | T/C | — | benign |
| rs181478757 | 6:109,197,433 | C/T | — | benign |
| rs143895116 | 6:109,197,435 | A/G | — | conflicting classifications of pathogenicity |
| rs751871044 | 6:109,197,536 | T/G | — | likely benign |
| rs755146711 | 6:109,197,538 | A/G | — | uncertain significance |
| rs768869041 | 6:109,220,947 | G/T | — | uncertain significance |
| rs186501123 | 6:109,220,972 | C/T | — | uncertain significance |
| rs373656754 | 6:109,220,981 | G/A | — | likely benign |
| rs1217176682 | 6:109,220,993 | A/C | — | uncertain significance |
| rs752222007 | 6:109,225,448 | C/T | — | uncertain significance |
| rs1562372417 | 6:109,225,609 | G/A | — | pathogenic |
| rs4945823 | 6:109,228,680 | T/A | — | — |
| rs2754824 | 6:109,230,448 | C/T | upstream gene variant | — |
| rs11153136 | 6:109,233,725 | T/C | — | benign |
| rs2754815 | 6:109,239,072 | T/C | intron variant | — |
| rs758099791 | 6:109,249,376 | C/T | — | uncertain significance |
| rs145704911 | 6:109,249,408 | G/A | — | uncertain significance |
| rs775864051 | 6:109,249,424 | C/T | — | uncertain significance |
| rs72933394 | 6:109,257,061 | G/T | — | — |
| rs2806353 | 6:109,257,688 | A/G | intron variant | — |
| rs911475 | 6:109,263,187 | C/G | — | — |
| rs2798641 | 6:109,268,050 | C/T | regulatory region variant | — |
| rs141068455 | 6:109,271,201 | G/C | — | — |
| rs755519656 | 6:109,274,249 | G/A | — | uncertain significance |
| rs61741720 | 6:109,274,276 | C/T | — | benign |
| rs2483694401 | 6:109,274,281 | A/C | — | uncertain significance |
| rs753812764 | 6:109,274,297 | G/A | — | uncertain significance |
| rs371652575 | 6:109,274,354 | C/T | — | uncertain significance |
| rs763924247 | 6:109,274,386 | C/G | — | uncertain significance |
| rs1010414745 | 6:109,274,402 | G/A | — | uncertain significance |
| rs746347815 | 6:109,274,416 | G/T | — | uncertain significance |
| rs41287540 | 6:109,274,418 | A/G | — | benign |
| rs371614341 | 6:109,274,426 | C/T | — | likely benign |
| rs369690998 | 6:109,274,465 | G/A | — | uncertain significance |
| rs199732181 | 6:109,274,505 | G/A | — | likely benign |
| rs760783374 | 6:109,274,522 | C/T | — | uncertain significance |
| rs113651966 | 6:109,274,527 | A/G | — | benign |
| rs780367511 | 6:109,274,537 | T/G | — | uncertain significance |
| rs780646638 | 6:109,274,549 | C/T | — | uncertain significance |
| rs12193858 | 6:109,277,908 | A/T | intron variant | — |
| rs12195848 | 6:109,279,105 | A/G | — | — |
| rs745850721 | 6:109,282,778 | A/T | — | uncertain significance |
| rs148788881 | 6:109,282,787 | T/C | — | uncertain significance |
| rs150814535 | 6:109,282,823 | C/T | — | uncertain significance |
| rs199601231 | 6:109,283,217 | T/C | — | uncertain significance |
| rs2483749031 | 6:109,283,241 | A/G | — | uncertain significance |
| rs144239422 | 6:109,283,298 | A/G | — | likely benign |
| rs2273669 | 6:109,285,189 | A/G | intron variant | — |
| rs370926614 | 6:109,285,481 | C/T | — | uncertain significance |
| rs1562435988 | 6:109,285,509 | T/A | — | pathogenic |
| rs76094073 | 6:109,288,036 | C/G | regulatory region variant | — |
| rs6568554 | 6:109,290,319 | C/A | intron variant | — |
| rs149101164 | 6:109,294,679 | C/G | — | uncertain significance |
| rs12196819 | 6:109,297,516 | G/A | downstream gene variant | — |
| rs10456862 | 6:109,299,089 | T/C | — | — |
| rs11153147 | 6:109,304,058 | A/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.