Variant (rsID / SNP)

rs117336883

rs117336883 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,275,554. 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: 11:1275554
Cytoband: 11p15.5
HGVS: NM_002458.3(MUC5B):c.15450C>T (p.Thr5150=)
Allele change: Synonymous_T5150T

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.