TTC39C
tetratricopeptide repeat domain 39C
Summary
Predicted to be involved in cilium assembly and otolith morphogenesis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1461385169 | 18:21,594,846 | C/T | — | uncertain significance |
| rs552231190 | 18:21,594,870 | G/A | — | uncertain significance |
| rs1005127509 | 18:21,594,950 | A/G | — | uncertain significance |
| rs10853615 | 18:21,638,509 | C/G | — | — |
| rs2043027 | 18:21,640,564 | G/A | regulatory region variant | — |
| rs777771290 | 18:21,649,142 | C/G | — | uncertain significance |
| rs200601152 | 18:21,660,623 | C/A | — | uncertain significance |
| rs1315768359 | 18:21,660,671 | G/C | — | uncertain significance |
| rs2511852618 | 18:21,660,707 | G/T | — | uncertain significance |
| rs140104738 | 18:21,660,776 | A/G | — | uncertain significance |
| rs539368375 | 18:21,660,783 | T/C | — | uncertain significance |
| rs550278973 | 18:21,660,809 | A/G | — | uncertain significance |
| rs1199307701 | 18:21,660,837 | G/A | — | uncertain significance |
| rs2511856206 | 18:21,662,948 | G/A | — | uncertain significance |
| rs2084395966 | 18:21,662,954 | A/T | — | uncertain significance |
| rs140420514 | 18:21,663,033 | A/G | — | uncertain significance |
| rs147825390 | 18:21,694,521 | C/G | — | uncertain significance |
| rs201906825 | 18:21,694,522 | A/G | — | uncertain significance |
| rs2511904377 | 18:21,698,102 | G/A | — | uncertain significance |
| rs62089609 | 18:21,698,118 | A/G | — | uncertain significance |
| rs764666906 | 18:21,698,173 | G/A | — | uncertain significance |
| rs762225333 | 18:21,698,185 | A/G | — | uncertain significance |
| rs201467118 | 18:21,703,804 | A/G | — | uncertain significance |
| rs766227571 | 18:21,705,433 | G/A | — | uncertain significance |
| rs72881750 | 18:21,705,440 | C/T | — | uncertain significance |
| rs1289229384 | 18:21,705,469 | G/A | — | uncertain significance |
| rs752555580 | 18:21,708,880 | T/C | — | uncertain significance |
| rs535810615 | 18:21,710,310 | C/T | — | uncertain significance |
| rs145032259 | 18:21,710,311 | G/A | — | uncertain significance |
| rs767706870 | 18:21,712,527 | G/C | — | uncertain significance |
| rs12607257 | 18:21,715,084 | A/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.