MAPT-AS1
MAPT antisense RNA 1
Summary
Involved in regulatory ncRNA-mediated gene silencing. Implicated in Parkinson's disease. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17690703 | 17:43,925,297 | C/T | downstream gene variant | — |
| rs8079387 | 17:43,926,777 | A/T | downstream gene variant | — |
| rs62054822 | 17:43,927,708 | A/C | — | — |
| rs885639 | 17:43,928,614 | T/G | downstream gene variant | — |
| rs55660209 | 17:43,932,173 | A/G | intron variant | — |
| rs10445365 | 17:43,932,789 | C/T | intron variant | — |
| rs10445366 | 17:43,932,797 | G/C | intron variant | — |
| rs10445367 | 17:43,932,798 | G/T | intron variant | — |
| rs7221167 | 17:43,933,307 | T/C | intron variant | — |
| rs142955985 | 17:43,933,790 | G/T | — | — |
| rs80209523 | 17:43,933,830 | G/A | — | — |
| rs242934 | 17:43,936,664 | G/T | — | — |
| rs55673092 | 17:43,938,882 | G/A | intron variant | — |
| rs56026232 | 17:43,939,399 | A/C | intron variant | — |
| rs79412431 | 17:43,940,021 | G/A | intron variant | — |
| rs886249 | 17:43,946,291 | A/G | intron variant | — |
| rs532403614 | 17:43,946,847 | C/T | — | — |
| rs75676226 | 17:43,947,171 | G/A | intron variant | — |
| rs6503451 | 17:43,948,347 | T/C | intron variant | — |
| rs9898399 | 17:43,950,322 | A/G | intron variant | — |
| rs62055489 | 17:43,950,441 | C/A | intron variant | — |
| rs62055494 | 17:43,953,016 | C/T | intron variant | — |
| rs111321973 | 17:43,953,170 | C/T | intron variant | — |
| rs2214258 | 17:43,953,719 | G/C | intron variant | — |
| rs56364632 | 17:43,956,642 | T/C | intron variant | — |
| rs55711631 | 17:43,958,431 | T/C | intron variant | — |
| rs62055544 | 17:43,964,539 | A/G | intron variant | — |
| rs62055545 | 17:43,964,561 | C/T | intron variant | — |
| rs62055546 | 17:43,964,567 | A/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.