Variant (rsID / SNP)
rs10277
rs10277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SQSTM1. Location: chromosome 5, position 179,264,731. Clinical significance in the table: Benign.
Reference-table entries
SQSTM1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:179264731
- Cytoband
- 5q35.3
- HGVS
- NM_003900.5(SQSTM1):c.*1138T>C
- Allele change
- Silent
Associated conditions / phenotypes
Paget disease of bone 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.