Variant (rsID / SNP)
rs56344012
rs56344012 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,276,467. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
MUC5BBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:1276467
- Cytoband
- 11p15.5
- HGVS
- NM_002458.3(MUC5B):c.15861A>G (p.Pro5287=)
- Allele change
- Synonymous_P5287P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.