Variant (rsID / SNP)
rs15783
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.
