Variant (rsID / SNP)
rs364569
rs364569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC10A. Location: chromosome 17, position 6,979,179. The table records no clinical significance for this variant.
Reference-table entries
CLEC10ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:6979179
- HGVS
- NM_182906.4,c.546T>C,p.Pro182Pro
- Allele change
- Synonymous_P182P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.