Variant (rsID / SNP)

rs61734215

rs61734215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC5B. Location: chromosome 11, position 1,281,932. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MUC5BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:1281932
Cytoband: 11p15.5
HGVS: NM_002458.3(MUC5B):c.17043C>T (p.Cys5681=)
Allele change: Synonymous_C5681C

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.