COL24A1
collagen type XXIV alpha 1 chain
Summary
This gene is a member of the collagen gene family and is thought to regulate type I collagen fibrillogenesis during fetal development. [provided by RefSeq, Mar 2017]
Known Variants99 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2524275392 | 1:86,196,246 | A/T | — | uncertain significance |
| rs765542339 | 1:86,196,257 | A/G | — | uncertain significance |
| rs1320712585 | 1:86,200,463 | A/C | — | uncertain significance |
| rs2524335453 | 1:86,200,553 | G/A | — | uncertain significance |
| rs2524373720 | 1:86,203,093 | C/G | — | uncertain significance |
| rs755480891 | 1:86,203,123 | T/G | — | uncertain significance |
| rs1664171648 | 1:86,203,141 | C/T | — | uncertain significance |
| rs2100842361 | 1:86,203,143 | A/G | — | uncertain significance |
| rs147783303 | 1:86,210,343 | A/G | splice region variant | — |
| rs2524476175 | 1:86,210,463 | T/A | — | uncertain significance |
| rs571556212 | 1:86,211,168 | C/T | — | uncertain significance |
| rs372445647 | 1:86,211,173 | T/C | — | uncertain significance |
| rs769517118 | 1:86,211,189 | T/C | — | uncertain significance |
| rs557759277 | 1:86,227,102 | G/A | — | uncertain significance |
| rs6692620 | 1:86,242,642 | T/G | — | — |
| rs751190840 | 1:86,246,913 | G/T | — | uncertain significance |
| rs2524998315 | 1:86,246,933 | T/G | — | uncertain significance |
| rs2525036483 | 1:86,249,208 | A/G | — | uncertain significance |
| rs768168420 | 1:86,249,800 | G/A | — | uncertain significance |
| rs1220375796 | 1:86,249,949 | C/T | — | uncertain significance |
| rs568711251 | 1:86,249,954 | C/T | — | likely benign |
| rs762151921 | 1:86,249,964 | T/A | — | uncertain significance |
| rs374842121 | 1:86,249,997 | C/T | — | likely benign |
| rs765308470 | 1:86,252,132 | C/T | — | likely benign |
| rs380654 | 1:86,264,025 | C/G | intron variant | — |
| rs313741 | 1:86,273,451 | A/T | intron variant | — |
| rs374137871 | 1:86,282,494 | G/C | — | uncertain significance |
| rs746139784 | 1:86,282,548 | T/C | — | uncertain significance |
| rs1031395804 | 1:86,282,575 | G/A | — | uncertain significance |
| rs375239501 | 1:86,283,721 | A/G | — | uncertain significance |
| rs187573768 | 1:86,289,213 | A/G | — | likely benign |
| rs1570761373 | 1:86,289,255 | C/A | — | uncertain significance |
| rs6698139 | 1:86,290,440 | A/G | — | — |
| rs4912446 | 1:86,302,708 | G/A | intron variant | — |
| rs183769998 | 1:86,304,282 | C/T | — | uncertain significance |
| rs375340928 | 1:86,306,930 | C/T | — | uncertain significance |
| rs146843570 | 1:86,306,960 | C/A | — | uncertain significance |
| rs773642410 | 1:86,307,798 | G/C | — | uncertain significance |
| rs201907029 | 1:86,313,349 | A/T | — | uncertain significance |
| rs763486597 | 1:86,313,400 | C/G | — | uncertain significance |
| rs781305166 | 1:86,315,077 | T/C | — | uncertain significance |
| rs200638964 | 1:86,334,212 | G/A | — | uncertain significance |
| rs74097605 | 1:86,334,302 | G/C | — | benign |
| rs200448368 | 1:86,340,342 | G/A | — | uncertain significance |
| rs767233670 | 1:86,340,355 | C/T | — | uncertain significance |
| rs1681013775 | 1:86,340,965 | C/G | — | uncertain significance |
| rs554002514 | 1:86,361,570 | G/A | — | uncertain significance |
| rs1038371530 | 1:86,361,720 | C/G | — | uncertain significance |
| rs1407268731 | 1:86,362,091 | C/G | — | uncertain significance |
| rs372408586 | 1:86,372,917 | G/A | — | uncertain significance |
| rs116405360 | 1:86,374,318 | G/T | — | benign |
| rs758737373 | 1:86,375,659 | C/G | — | uncertain significance |
| rs781239648 | 1:86,375,680 | G/A | — | uncertain significance |
| rs912655571 | 1:86,377,074 | T/C | — | uncertain significance |
| rs1685350844 | 1:86,377,080 | C/T | — | uncertain significance |
| rs183469380 | 1:86,426,944 | T/G | — | uncertain significance |
| rs566031608 | 1:86,428,553 | A/G | — | — |
| rs749471801 | 1:86,437,042 | G/A | — | uncertain significance |
| rs573444 | 1:86,438,019 | T/A | — | — |
| rs774125436 | 1:86,453,307 | G/A | — | uncertain significance |
| rs764259665 | 1:86,482,886 | C/T | — | uncertain significance |
| rs11161721 | 1:86,487,914 | C/A | intron variant | — |
| rs371662746 | 1:86,487,924 | G/A | — | uncertain significance |
| rs369573090 | 1:86,487,954 | G/A | — | uncertain significance |
| rs199668151 | 1:86,487,957 | C/A | — | uncertain significance |
| rs759111563 | 1:86,497,565 | A/C | — | uncertain significance |
| rs762501445 | 1:86,497,580 | G/A | — | uncertain significance |
| rs2524640158 | 1:86,512,534 | C/T | — | uncertain significance |
| rs774694829 | 1:86,523,649 | C/T | — | uncertain significance |
| rs528414070 | 1:86,529,418 | G/A | — | uncertain significance |
| rs6666986 | 1:86,531,456 | A/T | — | — |
| rs745549731 | 1:86,554,870 | A/C | — | uncertain significance |
| rs775172424 | 1:86,554,874 | C/T | — | uncertain significance |
| rs1156815742 | 1:86,578,297 | G/C | — | uncertain significance |
| rs370046426 | 1:86,581,009 | C/T | — | uncertain significance |
| rs6697461 | 1:86,583,237 | G/A | intron variant | — |
| rs187114451 | 1:86,590,635 | C/T | — | uncertain significance |
| rs774163714 | 1:86,590,721 | T/C | — | uncertain significance |
| rs1448025250 | 1:86,590,800 | T/A | — | uncertain significance |
| rs201337043 | 1:86,590,955 | C/T | — | uncertain significance |
| rs200901529 | 1:86,591,105 | T/C | — | likely benign |
| rs200800459 | 1:86,591,147 | G/T | — | uncertain significance |
| rs2525781629 | 1:86,591,157 | T/C | — | uncertain significance |
| rs1396091286 | 1:86,591,165 | G/A | — | uncertain significance |
| rs759740427 | 1:86,591,210 | G/A | — | likely benign |
| rs376018448 | 1:86,591,219 | T/C | — | uncertain significance |
| rs754600784 | 1:86,591,237 | G/A | — | uncertain significance |
| rs778227592 | 1:86,591,274 | G/T | — | uncertain significance |
| rs117871299 | 1:86,591,355 | A/G | — | benign |
| rs185528749 | 1:86,591,417 | C/T | — | benign |
| rs375785844 | 1:86,591,511 | T/C | — | likely benign |
| rs1362651577 | 1:86,591,517 | T/C | — | uncertain significance |
| rs1648227677 | 1:86,591,675 | T/C | — | uncertain significance |
| rs375692742 | 1:86,591,721 | C/T | — | uncertain significance |
| rs549789713 | 1:86,591,856 | C/G | — | uncertain significance |
| rs148644471 | 1:86,600,011 | T/C | — | — |
| rs1333153354 | 1:86,611,832 | C/T | — | uncertain significance |
| rs12068500 | 1:86,614,151 | G/T | intron variant | — |
| rs772334185 | 1:86,622,036 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.