DISP3
dispatched RND transporter family member 3
Summary
Involved in negative regulation of neuron differentiation; positive regulation of lipid metabolic process; and positive regulation of neural precursor cell proliferation. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants51 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201953977 | 1:11,561,057 | C/T | — | benign |
| rs41274528 | 1:11,561,164 | G/A | — | benign |
| rs758490195 | 1:11,561,170 | G/A | — | uncertain significance |
| rs3738159 | 1:11,561,200 | C/G | — | benign |
| rs202214902 | 1:11,561,257 | A/G | — | benign |
| rs375851130 | 1:11,561,546 | G/A | — | likely benign |
| rs2817580 | 1:11,561,593 | G/A | — | benign |
| rs143054501 | 1:11,561,600 | G/T | — | benign |
| rs780588416 | 1:11,561,634 | C/T | — | likely benign |
| rs753032518 | 1:11,561,682 | G/T | — | uncertain significance |
| rs183856902 | 1:11,561,692 | G/T | — | benign |
| rs372733155 | 1:11,561,763 | C/T | — | likely benign |
| rs371768702 | 1:11,561,931 | C/T | — | likely benign |
| rs12144924 | 1:11,561,937 | C/T | — | benign |
| rs60362998 | 1:11,562,913 | C/T | — | benign |
| rs201843567 | 1:11,570,666 | T/C | — | — |
| rs191060565 | 1:11,576,065 | C/T | — | benign |
| rs41274532 | 1:11,576,094 | G/A | — | likely benign |
| rs576463466 | 1:11,576,167 | C/T | — | likely benign |
| rs17036950 | 1:11,576,206 | C/T | — | benign |
| rs139045678 | 1:11,576,223 | G/A | — | likely benign |
| rs2072994 | 1:11,579,470 | A/G | — | benign |
| rs2072993 | 1:11,579,504 | G/C | — | benign |
| rs755313631 | 1:11,579,508 | C/T | — | likely benign |
| rs374016674 | 1:11,579,795 | C/T | — | likely benign |
| rs201408187 | 1:11,579,858 | C/T | — | likely benign |
| rs115032543 | 1:11,584,109 | C/G | — | benign |
| rs191852506 | 1:11,585,229 | G/A | — | benign |
| rs371821490 | 1:11,585,322 | C/T | — | uncertain significance |
| rs375072553 | 1:11,585,339 | G/A | — | likely benign |
| rs1642429384 | 1:11,586,756 | A/G | — | uncertain significance |
| rs199664959 | 1:11,586,772 | T/C | — | uncertain significance |
| rs374613319 | 1:11,586,834 | C/A | — | likely benign |
| rs77546140 | 1:11,589,872 | C/T | — | benign |
| rs2076468 | 1:11,589,911 | G/A | — | benign |
| rs201563606 | 1:11,589,914 | G/A | — | likely benign |
| rs200940112 | 1:11,589,979 | G/A | — | likely benign |
| rs762520292 | 1:11,589,985 | G/A | — | uncertain significance |
| rs767614532 | 1:11,590,982 | A/G | — | uncertain significance |
| rs377572784 | 1:11,591,051 | G/A | — | uncertain significance |
| rs148058598 | 1:11,591,618 | G/A | — | likely benign |
| rs146256525 | 1:11,594,563 | C/T | — | likely benign |
| rs140072373 | 1:11,594,593 | C/T | — | likely benign |
| rs41274536 | 1:11,595,087 | C/T | — | likely benign |
| rs41274538 | 1:11,595,185 | C/T | — | likely benign |
| rs3891105 | 1:11,595,572 | C/T | — | benign |
| rs2594310 | 1:11,596,455 | C/T | — | benign |
| rs201313405 | 1:11,596,500 | C/T | — | likely benign |
| rs184682642 | 1:11,596,629 | C/T | — | benign |
| rs370473756 | 1:11,596,633 | C/T | — | uncertain significance |
| rs112529124 | 1:11,596,725 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.