Variant (rsID / SNP)
rs2523897
rs2523897 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC22. Location: chromosome 6, position 30,993,958. The table records no clinical significance for this variant.
Reference-table entries
MUC22Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30993958
- HGVS
- NM_001318484.1,c.759A>G,p.Ala253Ala
- Allele change
- Synonymous_A250A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.