Variant (rsID / SNP)

rs73163759

rs73163759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC3A. Location: chromosome 7, position 100,552,536. The table records no clinical significance for this variant.

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Reference-table entries

MUC3ANot classified

Variant type: synonymous_variant
Chromosome / position: 7:100552536
HGVS: NM_005960.2,c.3108T>C,p.Ser1036Ser
Allele change: Synonymous_S1039S

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.