Variant (rsID / SNP)
rs3182911
rs3182911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COPS3. Location: chromosome 17, position 17,168,164. The table records no clinical significance for this variant.
Reference-table entries
COPS3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:17168164
- HGVS
- NM_003653.4,c.573C>T,p.Ile191Ile
- Allele change
- Synonymous_I61I
Associated conditions / phenotypes
Synonymous_I124I|Synonymous_I86I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.