ATXN7L1
ataxin 7 like 1
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs182409100 | 7:105,250,980 | C/T | — | uncertain significance |
| rs373477495 | 7:105,251,031 | A/G | — | uncertain significance |
| rs190958070 | 7:105,254,357 | G/T | — | uncertain significance |
| rs1490376676 | 7:105,254,365 | G/A | — | uncertain significance |
| rs2485340229 | 7:105,254,389 | T/C | — | uncertain significance |
| rs1250370724 | 7:105,254,513 | G/T | — | uncertain significance |
| rs769368632 | 7:105,254,524 | G/A | — | uncertain significance |
| rs192664230 | 7:105,254,577 | G/A | — | uncertain significance |
| rs761335657 | 7:105,254,602 | C/T | — | uncertain significance |
| rs562318903 | 7:105,254,619 | G/A | — | uncertain significance |
| rs2485341748 | 7:105,254,677 | T/G | — | uncertain significance |
| rs374076648 | 7:105,254,872 | C/T | — | uncertain significance |
| rs1312557744 | 7:105,254,888 | G/T | — | uncertain significance |
| rs778680974 | 7:105,254,964 | G/A | — | uncertain significance |
| rs923875758 | 7:105,255,040 | T/C | — | uncertain significance |
| rs561281717 | 7:105,255,112 | T/A | — | uncertain significance |
| rs2485343809 | 7:105,255,114 | T/C | — | uncertain significance |
| rs776428976 | 7:105,255,202 | C/T | — | uncertain significance |
| rs896651515 | 7:105,255,205 | G/C | — | uncertain significance |
| rs1423279732 | 7:105,255,217 | G/A | — | uncertain significance |
| rs551562834 | 7:105,260,678 | C/T | — | uncertain significance |
| rs768565377 | 7:105,260,704 | C/T | — | uncertain significance |
| rs1249608840 | 7:105,260,737 | C/T | — | uncertain significance |
| rs1209251634 | 7:105,264,524 | C/T | — | uncertain significance |
| rs990183793 | 7:105,264,578 | C/T | — | uncertain significance |
| rs765522233 | 7:105,264,673 | T/C | — | uncertain significance |
| rs748063114 | 7:105,264,688 | C/A | — | uncertain significance |
| rs10242311 | 7:105,273,720 | A/C | intron variant | — |
| rs1488734994 | 7:105,278,921 | T/C | — | likely benign |
| rs556888064 | 7:105,278,947 | T/G | — | uncertain significance |
| rs982970743 | 7:105,278,959 | A/G | — | uncertain significance |
| rs2484755588 | 7:105,279,001 | A/G | — | uncertain significance |
| rs1223487442 | 7:105,279,010 | T/C | — | uncertain significance |
| rs1453738063 | 7:105,279,016 | T/A | — | uncertain significance |
| rs775074734 | 7:105,279,974 | G/C | — | uncertain significance |
| rs1163433391 | 7:105,279,980 | A/G | — | uncertain significance |
| rs11983798 | 7:105,281,188 | G/A | intron variant | — |
| rs2484765631 | 7:105,283,312 | T/C | — | uncertain significance |
| rs751898584 | 7:105,283,336 | T/G | — | uncertain significance |
| rs375510569 | 7:105,283,444 | C/T | — | uncertain significance |
| rs201285335 | 7:105,283,493 | G/T | — | uncertain significance |
| rs371940751 | 7:105,283,506 | T/C | — | uncertain significance |
| rs2484766232 | 7:105,283,528 | G/C | — | uncertain significance |
| rs2484766238 | 7:105,283,530 | T/C | — | uncertain significance |
| rs1028354222 | 7:105,305,591 | G/A | — | uncertain significance |
| rs1170997616 | 7:105,305,669 | G/A | — | uncertain significance |
| rs758332065 | 7:105,305,703 | G/C | — | uncertain significance |
| rs146971766 | 7:105,429,124 | T/C | — | uncertain significance |
| rs187960185 | 7:105,437,095 | T/C | regulatory region variant | — |
| rs2485168078 | 7:105,516,288 | T/G | — | uncertain significance |
| rs2485168106 | 7:105,516,300 | C/G | — | uncertain significance |
| rs2485169249 | 7:105,516,841 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.