RIOX2
ribosomal oxygenase 2
Summary
MINA is a c-Myc (MYC; MIM 190080) target gene that may play a role in cell proliferation or regulation of cell growth. (Tsuneoka et al., 2002 [PubMed 12091391]; Zhang et al., 2005 [PubMed 15897898]).[supplied by OMIM, May 2008]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761388474 | 3:97,664,041 | A/C | — | uncertain significance |
| rs1475611209 | 3:97,664,158 | T/C | — | uncertain significance |
| rs557264232 | 3:97,664,174 | G/A | — | uncertain significance |
| rs2040329013 | 3:97,664,176 | A/C | — | uncertain significance |
| rs150618232 | 3:97,664,177 | G/A | — | uncertain significance |
| rs1460097623 | 3:97,664,186 | A/C | — | uncertain significance |
| rs1037111656 | 3:97,664,666 | C/A | — | uncertain significance |
| rs770506396 | 3:97,664,675 | C/G | — | uncertain significance |
| rs117990049 | 3:97,666,281 | G/C | — | uncertain significance |
| rs756941097 | 3:97,666,287 | T/C | — | uncertain significance |
| rs149644546 | 3:97,668,717 | G/A | — | likely benign |
| rs959662016 | 3:97,668,720 | G/C | — | uncertain significance |
| rs147454535 | 3:97,668,727 | G/A | — | uncertain significance |
| rs1395653413 | 3:97,668,745 | T/C | — | likely benign |
| rs200318327 | 3:97,668,753 | T/C | — | uncertain significance |
| rs1161176594 | 3:97,668,763 | C/T | — | uncertain significance |
| rs147195087 | 3:97,668,781 | T/C | — | uncertain significance |
| rs747442689 | 3:97,668,828 | C/T | — | uncertain significance |
| rs1385927779 | 3:97,668,837 | G/T | — | uncertain significance |
| rs555214241 | 3:97,668,838 | C/A | — | uncertain significance |
| rs832078 | 3:97,669,039 | C/T | intron variant | — |
| rs191961172 | 3:97,669,346 | A/C | intron variant | — |
| rs750184478 | 3:97,669,644 | G/A | — | uncertain significance |
| rs1236973619 | 3:97,669,652 | C/T | — | uncertain significance |
| rs758683491 | 3:97,669,653 | C/T | — | uncertain significance |
| rs762443916 | 3:97,669,700 | G/A | — | uncertain significance |
| rs750869465 | 3:97,669,703 | A/G | — | uncertain significance |
| rs199621662 | 3:97,669,710 | C/T | — | uncertain significance |
| rs17374916 | 3:97,671,742 | A/G | intron variant | — |
| rs9879532 | 3:97,672,076 | C/T | regulatory region variant | — |
| rs200630521 | 3:97,673,261 | C/T | — | uncertain significance |
| rs763141665 | 3:97,677,923 | C/A | — | uncertain significance |
| rs371041407 | 3:97,677,928 | C/A | — | uncertain significance |
| rs373581249 | 3:97,677,945 | C/T | — | uncertain significance |
| rs749722283 | 3:97,677,980 | T/C | — | uncertain significance |
| rs832081 | 3:97,680,074 | A/G | intron variant | — |
| rs557077258 | 3:97,680,455 | G/A | — | uncertain significance |
| rs201005276 | 3:97,680,498 | C/T | — | uncertain significance |
| rs377296377 | 3:97,680,536 | A/G | — | uncertain significance |
| rs9853899 | 3:97,685,329 | G/A | intron variant | — |
| rs1166271469 | 3:97,686,009 | A/C | — | uncertain significance |
| rs143860415 | 3:97,686,032 | G/T | — | uncertain significance |
| rs746870428 | 3:97,686,127 | C/T | — | uncertain significance |
| rs752086047 | 3:97,686,128 | G/A | — | uncertain significance |
| rs1472887328 | 3:97,686,137 | T/C | — | uncertain significance |
| rs768002152 | 3:97,686,158 | T/C | — | uncertain significance |
| rs2530589385 | 3:97,686,236 | T/C | — | uncertain significance |
| rs144762367 | 3:97,686,251 | G/C | — | uncertain significance |
| rs2530590509 | 3:97,686,347 | A/T | — | uncertain significance |
| rs759786970 | 3:97,686,368 | A/C | — | likely benign |
| rs552425813 | 3:97,686,391 | G/A | — | uncertain significance |
| rs4857304 | 3:97,690,323 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.