MYNN
myoneurin
Summary
This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010]
Known Variants21 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28649851 | 3:169,489,312 | A/C | — | — |
| rs10936599 | 3:169,492,101 | C/T | synonymous variant | association |
| rs757082996 | 3:169,492,169 | T/C | — | uncertain significance |
| rs758173459 | 3:169,492,232 | G/A | — | uncertain significance |
| rs200309187 | 3:169,492,340 | A/C | — | uncertain significance |
| rs3950296 | 3:169,493,283 | C/G | downstream gene variant | — |
| rs1881966 | 3:169,495,940 | G/C | coding sequence variant | — |
| rs749066571 | 3:169,496,839 | A/G | — | uncertain significance |
| rs771045925 | 3:169,496,840 | A/C | — | uncertain significance |
| rs762160662 | 3:169,496,867 | A/C | — | uncertain significance |
| rs761396977 | 3:169,496,965 | G/T | — | uncertain significance |
| rs756358574 | 3:169,497,038 | T/C | — | uncertain significance |
| rs1253209104 | 3:169,497,047 | C/G | — | uncertain significance |
| rs763359355 | 3:169,497,074 | A/T | — | uncertain significance |
| rs758209090 | 3:169,497,127 | G/A | — | uncertain significance |
| rs1051880004 | 3:169,497,308 | C/G | — | uncertain significance |
| rs1317082 | 3:169,497,585 | A/G | coding sequence variant | — |
| rs2474290930 | 3:169,498,509 | A/G | — | uncertain significance |
| rs3772190 | 3:169,500,487 | G/C | — | — |
| rs374143807 | 3:169,502,430 | G/A | — | uncertain significance |
| rs771584188 | 3:169,504,255 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.