COL26A1
collagen type XXVI alpha 1 chain
Summary
This gene encodes a protein containing an emilin domain and two collagen stretches. This gene may be associated with aspirin-intolerant asthma. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2013]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1021720147 | 7:101,006,341 | G/A | — | uncertain significance |
| rs749947111 | 7:101,006,419 | G/A | — | uncertain significance |
| rs1375550165 | 7:101,006,462 | C/G | — | uncertain significance |
| rs754260938 | 7:101,011,866 | A/G | — | — |
| rs13229821 | 7:101,019,039 | T/A | — | — |
| rs11772848 | 7:101,044,030 | G/A | intron variant | — |
| rs369792846 | 7:101,063,320 | C/T | — | uncertain significance |
| rs58441332 | 7:101,069,144 | A/C | — | — |
| rs13245979 | 7:101,070,772 | T/G | intron variant | — |
| rs527493762 | 7:101,076,030 | C/T | — | — |
| rs534693155 | 7:101,081,274 | A/G | — | — |
| rs181832531 | 7:101,084,235 | C/T | intron variant | — |
| rs2484806061 | 7:101,090,973 | C/T | — | uncertain significance |
| rs372441035 | 7:101,091,009 | C/T | — | uncertain significance |
| rs553286849 | 7:101,099,859 | C/T | — | — |
| rs17135437 | 7:101,115,994 | C/T | intron variant | — |
| rs73712171 | 7:101,129,765 | G/A | — | — |
| rs181514970 | 7:101,173,116 | G/A | intron variant | — |
| rs369433656 | 7:101,176,402 | G/A | — | uncertain significance |
| rs769091413 | 7:101,183,247 | C/T | — | uncertain significance |
| rs2485020996 | 7:101,183,289 | C/T | — | uncertain significance |
| rs200435737 | 7:101,183,304 | G/T | — | uncertain significance |
| rs770329760 | 7:101,183,318 | A/C | — | uncertain significance |
| rs376460376 | 7:101,183,319 | C/T | — | uncertain significance |
| rs1288422262 | 7:101,185,308 | C/T | — | — |
| rs749719561 | 7:101,187,281 | C/T | — | uncertain significance |
| rs774357671 | 7:101,187,285 | C/T | — | uncertain significance |
| rs764856083 | 7:101,187,311 | G/C | — | uncertain significance |
| rs1795674547 | 7:101,187,320 | C/G | — | uncertain significance |
| rs1194756803 | 7:101,187,348 | C/G | — | uncertain significance |
| rs573223764 | 7:101,187,372 | C/T | — | uncertain significance |
| rs572378566 | 7:101,188,634 | C/T | — | uncertain significance |
| rs191288309 | 7:101,188,640 | C/T | — | uncertain significance |
| rs2485035260 | 7:101,188,669 | C/T | — | uncertain significance |
| rs371036537 | 7:101,188,754 | C/T | — | uncertain significance |
| rs201322022 | 7:101,190,442 | G/A | — | uncertain significance |
| rs754486613 | 7:101,190,505 | C/A | — | uncertain significance |
| rs541739687 | 7:101,192,455 | C/A | — | uncertain significance |
| rs930679912 | 7:101,192,493 | C/A | — | uncertain significance |
| rs199553591 | 7:101,199,090 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.