Variant (rsID / SNP)
rs4248153
rs4248153 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 31,002,527. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:31002527
- HGVS
- NM_001318484.1,c.5143A>G,p.Asn1715Asp
- Allele change
- Missense_N1712D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.