TTC27
tetratricopeptide repeat domain 27
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747477414 | 2:32,853,369 | C/T | — | uncertain significance |
| rs765933012 | 2:32,855,590 | A/G | — | uncertain significance |
| rs2529126879 | 2:32,855,595 | G/A | — | uncertain significance |
| rs1272170901 | 2:32,855,635 | C/T | — | uncertain significance |
| rs768795399 | 2:32,855,720 | G/C | — | uncertain significance |
| rs200957498 | 2:32,855,761 | C/T | — | likely benign |
| rs769247042 | 2:32,859,010 | C/T | — | uncertain significance |
| rs201760629 | 2:32,859,017 | T/C | — | uncertain significance |
| rs1664314799 | 2:32,859,043 | T/C | — | likely benign |
| rs2151859166 | 2:32,859,044 | C/T | — | uncertain significance |
| rs528239582 | 2:32,863,606 | C/T | — | — |
| rs200824102 | 2:32,865,407 | C/T | — | likely benign |
| rs371771501 | 2:32,865,451 | G/A | — | likely benign |
| rs1031261 | 2:32,865,521 | G/C | intron variant | — |
| rs773452993 | 2:32,875,255 | C/T | — | uncertain significance |
| rs183477728 | 2:32,879,793 | C/T | intron variant | — |
| rs778130861 | 2:32,889,393 | G/T | — | uncertain significance |
| rs1055909446 | 2:32,889,403 | C/T | — | uncertain significance |
| rs1665684437 | 2:32,889,442 | C/T | — | uncertain significance |
| rs369574514 | 2:32,889,532 | C/T | — | uncertain significance |
| rs370351320 | 2:32,891,722 | C/T | — | uncertain significance |
| rs879728796 | 2:32,891,723 | G/A | — | uncertain significance |
| rs1382552118 | 2:32,891,752 | A/G | — | uncertain significance |
| rs143908434 | 2:32,891,769 | G/C | — | uncertain significance |
| rs146281194 | 2:32,891,788 | A/C | — | uncertain significance |
| rs1395367554 | 2:32,891,824 | C/T | — | uncertain significance |
| rs35725580 | 2:32,894,928 | A/C | — | — |
| rs757184099 | 2:32,897,345 | G/A | — | uncertain significance |
| rs1447186932 | 2:32,897,369 | A/C | — | uncertain significance |
| rs770174228 | 2:32,897,377 | A/G | — | uncertain significance |
| rs141160099 | 2:32,903,988 | C/T | — | uncertain significance |
| rs72787553 | 2:32,919,113 | T/C | intron variant | — |
| rs759291658 | 2:32,927,904 | A/G | — | uncertain significance |
| rs1386580863 | 2:32,927,911 | C/A | — | uncertain significance |
| rs535235861 | 2:32,927,937 | C/T | — | uncertain significance |
| rs200173708 | 2:32,958,916 | G/A | — | uncertain significance |
| rs563562841 | 2:32,958,917 | A/G | — | uncertain significance |
| rs2529452960 | 2:32,958,953 | T/C | — | uncertain significance |
| rs142785786 | 2:32,961,762 | G/A | — | uncertain significance |
| rs535351600 | 2:32,961,801 | G/C | — | uncertain significance |
| rs370124809 | 2:32,961,802 | T/G | — | uncertain significance |
| rs1351027128 | 2:32,961,816 | T/C | — | uncertain significance |
| rs973994202 | 2:32,961,833 | A/G | — | uncertain significance |
| rs112137907 | 2:32,961,878 | G/A | — | uncertain significance |
| rs762694296 | 2:32,983,488 | C/T | — | uncertain significance |
| rs751228170 | 2:32,983,497 | C/T | — | uncertain significance |
| rs1261131202 | 2:32,983,541 | G/C | — | uncertain significance |
| rs201317794 | 2:32,983,560 | C/T | — | uncertain significance |
| rs762752840 | 2:32,983,564 | C/G | — | uncertain significance |
| rs775054245 | 2:33,002,970 | G/A | — | uncertain significance |
| rs775053927 | 2:33,003,023 | G/T | — | uncertain significance |
| rs776065560 | 2:33,003,036 | C/G | — | uncertain significance |
| rs769381715 | 2:33,007,702 | G/A | — | uncertain significance |
| rs777400596 | 2:33,007,703 | C/A | — | uncertain significance |
| rs766483659 | 2:33,012,095 | A/G | — | uncertain significance |
| rs144557313 | 2:33,012,142 | G/A | — | uncertain significance |
| rs748497472 | 2:33,012,143 | T/C | — | uncertain significance |
| rs532095651 | 2:33,012,193 | C/T | — | uncertain significance |
| rs2529711082 | 2:33,036,119 | T/C | — | uncertain significance |
| rs1197648924 | 2:33,036,236 | A/G | — | uncertain significance |
| rs772520508 | 2:33,042,602 | G/A | — | uncertain significance |
| rs370426638 | 2:33,045,946 | A/G | — | uncertain significance |
| rs889756340 | 2:33,045,992 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.