ATXN7L2
ataxin 7 like 2
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2524044682 | 1:110,026,600 | G/A | — | uncertain significance |
| rs764076726 | 1:110,026,665 | C/G | — | uncertain significance |
| rs767799921 | 1:110,026,675 | G/A | — | uncertain significance |
| rs2524064872 | 1:110,029,149 | G/T | — | uncertain significance |
| rs762687905 | 1:110,029,655 | C/G | — | uncertain significance |
| rs201678517 | 1:110,029,664 | C/T | — | uncertain significance |
| rs572464653 | 1:110,029,791 | G/A | — | uncertain significance |
| rs910593265 | 1:110,030,331 | C/T | — | uncertain significance |
| rs1144593 | 1:110,030,945 | A/G | regulatory region variant | — |
| rs2524079777 | 1:110,031,020 | T/G | — | uncertain significance |
| rs12049330 | 1:110,031,188 | T/A | — | — |
| rs1203222230 | 1:110,031,481 | C/A | — | uncertain significance |
| rs199993090 | 1:110,031,523 | G/A | — | uncertain significance |
| rs146370673 | 1:110,031,553 | C/T | — | uncertain significance |
| rs766137202 | 1:110,031,607 | G/A | — | uncertain significance |
| rs150011982 | 1:110,031,610 | C/T | — | uncertain significance |
| rs145282300 | 1:110,031,653 | C/T | — | uncertain significance |
| rs751808036 | 1:110,032,562 | T/G | — | uncertain significance |
| rs562739459 | 1:110,032,640 | C/T | — | uncertain significance |
| rs200119345 | 1:110,032,683 | G/A | — | uncertain significance |
| rs778459954 | 1:110,032,703 | C/G | — | uncertain significance |
| rs377314546 | 1:110,032,719 | A/G | — | uncertain significance |
| rs766504933 | 1:110,032,948 | G/A | — | uncertain significance |
| rs761113751 | 1:110,033,591 | C/G | — | uncertain significance |
| rs1253021871 | 1:110,033,593 | T/A | — | uncertain significance |
| rs763920807 | 1:110,033,626 | A/T | — | likely benign |
| rs370063225 | 1:110,033,720 | G/C | — | uncertain significance |
| rs1043682697 | 1:110,033,758 | T/C | — | uncertain significance |
| rs766259912 | 1:110,033,813 | C/T | — | uncertain significance |
| rs542068728 | 1:110,033,903 | A/G | — | uncertain significance |
| rs563921907 | 1:110,034,061 | C/A | — | uncertain significance |
| rs780938693 | 1:110,034,065 | T/A | — | uncertain significance |
| rs150258486 | 1:110,034,107 | A/G | — | uncertain significance |
| rs759008632 | 1:110,034,109 | G/A | — | uncertain significance |
| rs774805295 | 1:110,034,164 | C/T | — | uncertain significance |
| rs2524111067 | 1:110,034,256 | G/A | — | uncertain significance |
| rs369441759 | 1:110,034,283 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.