TTC34
tetratricopeptide repeat domain 34
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs764511411 | 1:2,572,842 | G/A | — | uncertain significance |
| rs769709808 | 1:2,572,871 | C/T | — | uncertain significance |
| rs928056503 | 1:2,572,907 | G/A | — | uncertain significance |
| rs965059894 | 1:2,572,966 | C/G | — | uncertain significance |
| rs921129916 | 1:2,572,970 | C/T | — | uncertain significance |
| rs1303871995 | 1:2,572,983 | C/A | — | uncertain significance |
| rs769825854 | 1:2,572,999 | G/C | — | likely benign |
| rs760218762 | 1:2,573,094 | G/C | — | uncertain significance |
| rs1638907586 | 1:2,573,117 | G/A | — | likely benign |
| rs773963798 | 1:2,573,120 | C/A | — | uncertain significance |
| rs562631002 | 1:2,573,121 | G/A | — | uncertain significance |
| rs541777946 | 1:2,573,184 | G/A | — | uncertain significance |
| rs774561401 | 1:2,573,234 | C/A | — | uncertain significance |
| rs527944346 | 1:2,573,241 | T/G | — | uncertain significance |
| rs772710901 | 1:2,573,330 | G/A | — | uncertain significance |
| rs550126719 | 1:2,573,334 | C/T | — | uncertain significance |
| rs894606686 | 1:2,575,713 | C/T | — | uncertain significance |
| rs758267296 | 1:2,575,719 | C/T | — | uncertain significance |
| rs1460810829 | 1:2,575,725 | G/A | — | uncertain significance |
| rs2522994835 | 1:2,575,732 | C/T | — | uncertain significance |
| rs2522996660 | 1:2,575,795 | T/C | — | uncertain significance |
| rs773496669 | 1:2,575,843 | G/A | — | uncertain significance |
| rs769483674 | 1:2,575,902 | G/C | — | uncertain significance |
| rs1046342121 | 1:2,575,909 | C/G | — | uncertain significance |
| rs180777014 | 1:2,576,779 | C/T | — | uncertain significance |
| rs778083580 | 1:2,576,786 | C/G | — | uncertain significance |
| rs2523000053 | 1:2,576,789 | T/G | — | uncertain significance |
| rs1639002070 | 1:2,576,909 | T/A | — | uncertain significance |
| rs575007693 | 1:2,576,938 | C/T | — | uncertain significance |
| rs1173030440 | 1:2,576,939 | G/A | — | uncertain significance |
| rs761501123 | 1:2,576,953 | A/G | — | uncertain significance |
| rs750327662 | 1:2,576,966 | C/G | — | uncertain significance |
| rs4648664 | 1:2,584,095 | A/T | — | — |
| rs547973018 | 1:2,628,854 | G/T | — | — |
| rs71632380 | 1:2,692,477 | G/A | — | — |
| rs551740211 | 1:2,700,189 | G/A | — | uncertain significance |
| rs764297828 | 1:2,700,207 | C/T | — | uncertain significance |
| rs1429174132 | 1:2,700,225 | G/A | — | uncertain significance |
| rs1342650153 | 1:2,700,242 | T/C | — | uncertain significance |
| rs2522220360 | 1:2,700,251 | G/C | — | uncertain significance |
| rs778533119 | 1:2,700,284 | C/T | — | uncertain significance |
| rs371838549 | 1:2,700,285 | G/A | — | uncertain significance |
| rs965920436 | 1:2,702,387 | C/A | — | uncertain significance |
| rs761299025 | 1:2,702,450 | C/T | — | uncertain significance |
| rs533573532 | 1:2,702,464 | C/T | — | uncertain significance |
| rs1018784951 | 1:2,702,512 | C/T | — | uncertain significance |
| rs577501461 | 1:2,702,519 | C/T | — | uncertain significance |
| rs546396984 | 1:2,702,531 | C/T | — | likely benign |
| rs370056680 | 1:2,702,532 | G/A | — | likely benign |
| rs1042224904 | 1:2,702,555 | C/T | — | uncertain significance |
| rs754188678 | 1:2,704,095 | C/T | — | uncertain significance |
| rs1242972073 | 1:2,704,161 | T/C | — | uncertain significance |
| rs1286164065 | 1:2,704,164 | A/G | — | uncertain significance |
| rs780715170 | 1:2,704,194 | G/A | — | uncertain significance |
| rs1022425489 | 1:2,704,203 | C/T | — | uncertain significance |
| rs775934260 | 1:2,704,258 | C/T | — | uncertain significance |
| rs760628555 | 1:2,704,261 | C/A | — | uncertain significance |
| rs55972083 | 1:2,704,918 | G/T | intron variant | — |
| rs565252018 | 1:2,706,093 | T/C | — | uncertain significance |
| rs1050362666 | 1:2,706,138 | G/C | — | uncertain significance |
| rs537229877 | 1:2,706,334 | G/C | — | likely benign |
| rs4648356 | 1:2,709,164 | C/A | upstream gene variant | — |
| rs897628 | 1:2,716,624 | C/G | — | — |
| rs61766525 | 1:2,717,333 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.