MEIS1
Meis homeobox 1
Summary
Homeobox genes, of which the most well-characterized category is represented by the HOX genes, play a crucial role in normal development. In addition, several homeoproteins are involved in neoplasia. This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1310247578 | 2:66,664,894 | G/A | — | uncertain significance |
| rs778204771 | 2:66,664,925 | G/A | — | uncertain significance |
| rs375684991 | 2:66,664,947 | A/C | — | likely benign |
| rs2466143891 | 2:66,664,968 | C/G | — | uncertain significance |
| rs558509818 | 2:66,665,063 | C/A | — | uncertain significance |
| rs2271856 | 2:66,667,186 | C/T | regulatory region variant | — |
| rs1671978928 | 2:66,668,567 | T/A | — | uncertain significance |
| rs753232642 | 2:66,670,118 | A/G | — | uncertain significance |
| rs11883967 | 2:66,673,862 | A/C | regulatory region variant | — |
| rs939136 | 2:66,677,531 | G/T | — | — |
| rs1519102 | 2:66,677,816 | G/A | — | — |
| rs62144048 | 2:66,710,578 | A/G | intron variant | — |
| rs12995572 | 2:66,725,070 | C/G | regulatory region variant | — |
| rs4300816 | 2:66,746,551 | C/T | intron variant | — |
| rs6724747 | 2:66,749,828 | G/C | — | — |
| rs4544423 | 2:66,750,017 | T/C | — | — |
| rs4233937 | 2:66,752,251 | A/G | intron variant | — |
| rs3891585 | 2:66,756,976 | A/G | intron variant | — |
| rs6710341 | 2:66,758,422 | A/G | regulatory region variant | — |
| rs11678354 | 2:66,760,079 | T/A | intron variant | — |
| rs12469063 | 2:66,764,308 | A/G | intron variant | — |
| rs10865355 | 2:66,764,997 | A/G | intron variant | — |
| rs9789535 | 2:66,765,578 | A/G | regulatory region variant | — |
| rs9798015 | 2:66,768,262 | C/T | intron variant | — |
| rs11897119 | 2:66,772,000 | T/A | — | — |
| rs2192954 | 2:66,777,521 | A/T | — | — |
| rs2300478 | 2:66,781,453 | T/G | intron variant | — |
| rs1675410948 | 2:66,795,797 | A/G | — | uncertain significance |
| rs758483192 | 2:66,795,839 | G/T | — | uncertain significance |
| rs73937957 | 2:66,795,857 | C/T | — | benign |
| rs1675412747 | 2:66,795,882 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.