Variant (rsID / SNP)
rs55657020
rs55657020 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,278,796. Clinical significance in the table: Benign.
Reference-table entries
MUC5BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:1278796
- Cytoband
- 11p15.5
- HGVS
- NM_002458.3(MUC5B):c.16306G>A (p.Val5436Met)
- Allele change
- Missense_V5436M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.