TARID
TCF21 antisense RNA inducing promoter demethylation
Known Variants11 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9402515 | 6:133,860,345 | A/G | upstream gene variant | — |
| rs9375969 | 6:133,867,802 | G/C | — | — |
| rs2636590 | 6:133,935,728 | G/A | intron variant | — |
| rs80176668 | 6:134,069,965 | A/G | regulatory region variant | — |
| rs76987554 | 6:134,080,855 | C/T | intron variant | — |
| rs9399078 | 6:134,179,581 | C/T | intron variant | — |
| rs2105092 | 6:134,184,972 | G/A | intron variant | — |
| rs12192720 | 6:134,195,719 | G/A | intron variant | — |
| rs12524865 | 6:134,196,674 | C/A | intron variant | — |
| rs6934010 | 6:134,203,010 | C/T | intron variant | — |
| rs6920657 | 6:134,206,202 | G/T | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.