Variant (rsID / SNP)

rs4963059

rs4963059 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,272,858. Clinical significance in the table: Benign.

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Reference-table entries

MUC5BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:1272858
Cytoband: 11p15.5
HGVS: NM_002458.3(MUC5B):c.14748C>T (p.Phe4916=)
Allele change: Synonymous_F4916F

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.