Variant (rsID / SNP)
rs1003645
rs1003645 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCL23. Location: chromosome 17, position 34,340,284. The table records no clinical significance for this variant.
Reference-table entries
CCL23Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:34340284
- HGVS
- NM_005064.6,c.367G>A,p.Val123Met
- Allele change
- Missense_V106M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.