Variant (rsID / SNP)
rs1061098
rs1061098 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCN5. Location: chromosome 20, position 43,356,156. The table records no clinical significance for this variant.
Reference-table entries
CCN5Not classified
- Variant type
- 3_prime_UTR_variant
- Chromosome / position
- 20:43356156
- HGVS
- NM_001323370.2,c.*208C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.