Variant (rsID / SNP)
rs4248154
rs4248154 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 31,002,616. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:31002616
- HGVS
- NM_001318484.1,c.5232C>T,p.His1744His
- Allele change
- Synonymous_H1741H
Associated conditions / phenotypes
Graves' Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.