Variant (rsID / SNP)
rs78692183
rs78692183 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,263,757. Clinical significance in the table: Benign.
Reference-table entries
MUC5BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:1263757
- Cytoband
- 11p15.5
- HGVS
- NM_002458.3(MUC5B):c.5647A>G (p.Ser1883Gly)
- Allele change
- Missense_S1883G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.