Annotation Detail
Information
- Associated Genes
- MTHFR
- Associated Variants
-
MTHFR c.*372A>C
(
ENST00000376585.6,
ENST00000376583.7,
ENST00000423400.7,
ENST00000376590.9,
ENST00000376592.6 )
MTHFR c.*372A>C ( ENST00000376583.7, ENST00000376585.6, ENST00000376590.9, ENST00000376592.6, ENST00000423400.7 ) - Associated Disease
- Homocystinuria due to methylene tetrahydrofolate reductase deficiency
- Source Database
- ClinVar
- Description
- NM_005957.5(MTHFR):c.*372A>C AND Homocystinuria due to methylene tetrahydrofolate reductase deficiency
- ClinVar Allele ID
- 276753
- ClinVar RefSeq Alternation Syntax
- NM_005957.5:c.*372A>C
- ClinVar RefSeq Alternation Syntax
- NM_001330358.2:c.*372A>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001523551
- ClinVar Disease
- Homocystinuria due to methylene tetrahydrofolate reductase deficiency
- Observed Origin Sample
- germline
Drugs