Annotation Detail
Information
- Associated Genes
- ARSA
- Associated Variants
-
ARSA c.979+1G>A
(
ENST00000216124.10,
ENST00000356098.9,
ENST00000395619.3,
ENST00000395621.7,
ENST00000453344.6 )
ARSA c.979+1G>A ( ENST00000216124.10, ENST00000356098.9, ENST00000395619.3, ENST00000395621.7, ENST00000453344.6 ) - Associated Disease
- metachromatic leukodystrophy
- Source Database
- ClinVar
- Description
- NM_000487.6(ARSA):c.979+1G>A AND Metachromatic leukodystrophy
- ClinVar Allele ID
- 187071
- ClinVar RefSeq Alternation Syntax
- NM_000487.6:c.979+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001362782.2:c.721+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085428.3:c.721+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085425.3:c.979+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085427.3:c.979+1G>A
- ClinVar RefSeq Alternation Syntax
- NM_001085426.3:c.979+1G>A
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-10-28
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000169323
- ClinVar Disease
- Metachromatic leukodystrophy
- Observed Origin Sample
- germline
- Observed Origin Sample
- inherited
- Observed Origin Sample
- unknown
Drugs