Variant (rsID / SNP)
rs12179536
rs12179536 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 30,993,590. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:30993590
- HGVS
- NM_001318484.1,c.391A>G,p.Ile131Val
- Allele change
- Missense_I128V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.