Variant (rsID / SNP)
rs1419664
rs1419664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 30,993,313. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30993313
- HGVS
- NM_001318484.1,c.114C>T,p.Ser38Ser
- Allele change
- Synonymous_S35S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.