Variant (rsID / SNP)
rs900641
rs900641 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALDH7A1. Location: chromosome 5, position 125,931,022. Clinical significance in the table: Benign.
Reference-table entries
ALDH7A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:125931022
- Cytoband
- 5q23.2
- HGVS
- NM_001182.4(ALDH7A1):c.-132A>C
- Allele change
- Silent
Associated conditions / phenotypes
Pyridoxine-dependent epilepsy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.