Variant (rsID / SNP)
rs710794
rs710794 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LYZ. Location: chromosome 12, position 69,747,177. Clinical significance in the table: Benign.
Reference-table entries
LYZBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:69747177
- Cytoband
- 12q15
- HGVS
- NM_000239.3(LYZ):c.*178C>T
- Allele change
- Silent
Associated conditions / phenotypes
Familial visceral amyloidosis, Ostertag type
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.