UNC5A
unc-5 netrin receptor A
Summary
UNC5A belongs to a family of netrin-1 (MIM 601614) receptors thought to mediate the chemorepulsive effect of netrin-1 on specific axons. For more information on UNC5 proteins, see UNC5C (MIM 603610).[supplied by OMIM, Apr 2004]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144524143 | 5:176,247,952 | T/G | intron variant | — |
| rs7705678 | 5:176,279,721 | C/G | — | — |
| rs575430416 | 5:176,281,145 | C/A | — | — |
| rs137863793 | 5:176,284,869 | G/A | intron variant | — |
| rs190998600 | 5:176,285,416 | G/T | intron variant | — |
| rs56402307 | 5:176,286,135 | C/T | intron variant | — |
| rs2532509427 | 5:176,289,664 | G/A | — | uncertain significance |
| rs148982495 | 5:176,289,717 | A/G | — | uncertain significance |
| rs375970937 | 5:176,289,720 | G/A | — | uncertain significance |
| rs1259498304 | 5:176,289,730 | A/C | — | uncertain significance |
| rs755629307 | 5:176,289,756 | G/A | — | uncertain significance |
| rs754588392 | 5:176,289,762 | G/A | — | uncertain significance |
| rs375724945 | 5:176,289,825 | C/T | — | uncertain significance |
| rs140306147 | 5:176,289,837 | G/A | — | uncertain significance |
| rs200004005 | 5:176,292,667 | C/T | intron variant | — |
| rs775312984 | 5:176,295,568 | G/A | — | uncertain significance |
| rs150169358 | 5:176,295,624 | G/C | — | uncertain significance |
| rs111351493 | 5:176,295,941 | G/A | — | uncertain significance |
| rs142434147 | 5:176,297,503 | C/T | — | uncertain significance |
| rs1758083899 | 5:176,297,518 | G/C | — | uncertain significance |
| rs150911396 | 5:176,301,013 | G/A | — | uncertain significance |
| rs1044341173 | 5:176,301,016 | G/A | — | uncertain significance |
| rs1214117265 | 5:176,301,024 | C/T | — | likely benign |
| rs2532534924 | 5:176,301,046 | G/C | — | uncertain significance |
| rs752966595 | 5:176,301,133 | G/A | — | uncertain significance |
| rs369754511 | 5:176,301,405 | G/A | — | uncertain significance |
| rs889510004 | 5:176,301,430 | C/T | — | uncertain significance |
| rs1041183670 | 5:176,301,456 | G/A | — | uncertain significance |
| rs146409898 | 5:176,301,463 | G/A | — | uncertain significance |
| rs761537189 | 5:176,304,222 | A/G | — | uncertain significance |
| rs760615400 | 5:176,304,544 | T/A | — | uncertain significance |
| rs755099198 | 5:176,304,576 | G/A | — | uncertain significance |
| rs148579650 | 5:176,305,018 | G/A | — | uncertain significance |
| rs377319758 | 5:176,305,297 | G/A | — | uncertain significance |
| rs769542258 | 5:176,305,555 | G/A | — | uncertain significance |
| rs765514327 | 5:176,305,602 | G/A | — | uncertain significance |
| rs2532546010 | 5:176,306,336 | C/G | — | uncertain significance |
| rs148900887 | 5:176,306,443 | C/T | — | likely benign |
| rs760813993 | 5:176,306,458 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.