MAP7D1
MAP7 domain containing 1
Summary
Predicted to be involved in microtubule cytoskeleton organization. Located in spindle. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs530814067 | 1:36,622,022 | G/A | — | uncertain significance |
| rs1644329788 | 1:36,622,028 | G/A | — | uncertain significance |
| rs745390462 | 1:36,622,056 | C/T | — | uncertain significance |
| rs11263862 | 1:36,632,051 | C/G | — | — |
| rs145462639 | 1:36,636,587 | C/T | — | likely benign |
| rs779828198 | 1:36,636,631 | C/T | — | uncertain significance |
| rs530295377 | 1:36,636,633 | A/C | — | likely benign |
| rs765600819 | 1:36,636,754 | C/T | — | uncertain significance |
| rs138447994 | 1:36,636,770 | C/T | — | uncertain significance |
| rs139650826 | 1:36,636,774 | G/A | — | benign |
| rs2296266 | 1:36,636,835 | C/T | — | benign |
| rs1384509886 | 1:36,636,848 | C/T | — | uncertain significance |
| rs756013396 | 1:36,636,872 | C/T | — | uncertain significance |
| rs1245331355 | 1:36,636,883 | G/C | — | uncertain significance |
| rs755121841 | 1:36,637,114 | A/C | — | uncertain significance |
| rs1238045023 | 1:36,637,159 | G/A | — | uncertain significance |
| rs142245111 | 1:36,638,104 | C/T | — | uncertain significance |
| rs140127558 | 1:36,638,116 | G/A | — | uncertain significance |
| rs544414202 | 1:36,638,135 | G/T | — | uncertain significance |
| rs117018122 | 1:36,638,146 | G/A | — | benign |
| rs758768532 | 1:36,638,178 | C/T | — | uncertain significance |
| rs375875834 | 1:36,638,182 | G/A | — | uncertain significance |
| rs780789428 | 1:36,638,199 | C/T | — | uncertain significance |
| rs545839803 | 1:36,638,968 | C/T | — | uncertain significance |
| rs2524932944 | 1:36,638,999 | A/G | — | uncertain significance |
| rs1242416418 | 1:36,639,002 | A/G | — | uncertain significance |
| rs774423816 | 1:36,639,033 | G/C | — | uncertain significance |
| rs200884547 | 1:36,640,516 | G/C | — | uncertain significance |
| rs2524945296 | 1:36,641,919 | C/G | — | uncertain significance |
| rs2524945540 | 1:36,641,959 | G/T | — | uncertain significance |
| rs778396406 | 1:36,642,000 | C/A | — | uncertain significance |
| rs1314380396 | 1:36,642,093 | T/C | — | uncertain significance |
| rs1570160339 | 1:36,642,099 | C/A | — | uncertain significance |
| rs113489132 | 1:36,642,153 | C/G | — | uncertain significance |
| rs780310575 | 1:36,642,154 | C/T | — | uncertain significance |
| rs768306601 | 1:36,642,163 | G/T | — | uncertain significance |
| rs780617848 | 1:36,642,165 | C/T | — | uncertain significance |
| rs1408838568 | 1:36,642,168 | C/T | — | uncertain significance |
| rs766850841 | 1:36,642,395 | C/G | — | uncertain significance |
| rs539606561 | 1:36,643,487 | G/A | — | uncertain significance |
| rs1270761227 | 1:36,643,596 | C/G | — | uncertain significance |
| rs781072648 | 1:36,643,635 | C/G | — | uncertain significance |
| rs763817876 | 1:36,643,652 | G/T | — | uncertain significance |
| rs1320551427 | 1:36,643,689 | G/C | — | uncertain significance |
| rs959471577 | 1:36,643,743 | C/T | — | likely benign |
| rs745465401 | 1:36,643,754 | A/C | — | uncertain significance |
| rs1425175411 | 1:36,643,777 | G/C | — | uncertain significance |
| rs764478271 | 1:36,643,794 | C/A | — | uncertain significance |
| rs780689136 | 1:36,644,055 | C/T | — | uncertain significance |
| rs1172164051 | 1:36,644,151 | C/T | — | uncertain significance |
| rs964149496 | 1:36,644,312 | G/C | — | uncertain significance |
| rs763642567 | 1:36,644,330 | C/T | — | uncertain significance |
| rs1393759096 | 1:36,644,574 | A/T | — | uncertain significance |
| rs373798227 | 1:36,644,914 | A/G | — | uncertain significance |
| rs1331389318 | 1:36,645,154 | C/G | — | uncertain significance |
| rs2524967131 | 1:36,645,272 | G/C | — | uncertain significance |
| rs201770066 | 1:36,645,291 | G/A | — | uncertain significance |
| rs769666030 | 1:36,645,558 | A/G | — | uncertain significance |
| rs768808449 | 1:36,645,574 | C/A | — | uncertain significance |
| rs2524969017 | 1:36,645,590 | A/G | — | uncertain significance |
| rs2524969166 | 1:36,645,627 | C/T | — | uncertain significance |
| rs768559148 | 1:36,645,657 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.