Variant (rsID / SNP)
rs1772719
rs1772719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALPL. Location: chromosome 1, position 21,904,374. Clinical significance in the table: Benign.
Reference-table entries
ALPLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:21904374
- Cytoband
- 1p36.12
- HGVS
- NM_000478.6(ALPL):c.*233A>C
- Allele change
- Silent
Associated conditions / phenotypes
Hypophosphatasia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.