LMNTD1
lamin tail domain containing 1
Summary
Predicted to act upstream of or within cell population proliferation. Predicted to be located in intermediate filament and nucleus. Predicted to be active in cytoplasm and nuclear envelope. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150520438 | 12:25,646,762 | T/C | regulatory region variant | — |
| rs747504355 | 12:25,671,744 | G/A | — | uncertain significance |
| rs750530049 | 12:25,671,762 | T/C | — | uncertain significance |
| rs151140890 | 12:25,671,837 | A/C | — | uncertain significance |
| rs1266230982 | 12:25,671,860 | G/A | — | uncertain significance |
| rs768195750 | 12:25,672,837 | T/C | — | uncertain significance |
| rs2549062417 | 12:25,672,861 | T/G | — | uncertain significance |
| rs772520318 | 12:25,672,949 | C/T | — | likely benign |
| rs777251354 | 12:25,672,972 | G/A | — | uncertain significance |
| rs759508652 | 12:25,672,973 | C/T | — | uncertain significance |
| rs1746328847 | 12:25,673,006 | T/C | — | likely benign |
| rs1368363450 | 12:25,679,052 | A/G | — | uncertain significance |
| rs766030891 | 12:25,679,079 | C/G | — | uncertain significance |
| rs2549092396 | 12:25,679,083 | A/T | — | uncertain significance |
| rs2549096152 | 12:25,679,724 | C/T | — | uncertain significance |
| rs535308374 | 12:25,679,791 | T/C | — | uncertain significance |
| rs192437605 | 12:25,679,830 | A/G | — | uncertain significance |
| rs139058419 | 12:25,679,848 | C/T | — | uncertain significance |
| rs367548196 | 12:25,699,467 | G/A | — | uncertain significance |
| rs1394341088 | 12:25,699,479 | G/T | — | uncertain significance |
| rs1252061279 | 12:25,702,316 | C/T | — | uncertain significance |
| rs537956454 | 12:25,703,516 | T/G | — | — |
| rs530661144 | 12:25,705,878 | C/T | — | uncertain significance |
| rs575007757 | 12:25,705,887 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.