Variant (rsID / SNP)
rs7315231
rs7315231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC9A. Location: chromosome 12, position 10,206,925. The table records no clinical significance for this variant.
Reference-table entries
CLEC9ANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:10206925
- HGVS
- NM_207345.4,c.147A>G,p.Thr49Thr
- Allele change
- Synonymous_T49T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.