Variant (rsID / SNP)
rs7672268
rs7672268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MANBA. Location: chromosome 4, position 103,552,858. Clinical significance in the table: Benign.
Reference-table entries
MANBABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:103552858
- Cytoband
- 4q24
- HGVS
- NM_005908.4(MANBA):c.*356G>A
- Allele change
- Silent
Associated conditions / phenotypes
Beta-D-mannosidosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.