Variant (rsID / SNP)
rs76248080
rs76248080 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCT4. Location: chromosome 2, position 62,100,380. The table records no clinical significance for this variant.
Reference-table entries
CCT4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:62100380
- HGVS
- NM_006430.4,c.966C>A,p.Ile322Ile
- Allele change
- Synonymous_I292I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.