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Variant (rsID / SNP)

rs15783

MUC15ANO3

rs15783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC15, ANO3. Location: chromosome 11, position 26,586,801. The table records no clinical significance for this variant.

Reference-table entries

MUC15Not classified
Variant type
missense_variant
Chromosome / position
11:26586801
HGVS
NM_001135091.2,c.686C>T,p.Thr229Ile
Allele change
Silent

Associated conditions / phenotypes

Dermatitis

Public references

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