Variant (rsID / SNP)
rs881711
rs881711 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBR3. Location: chromosome 21, position 37,507,745. The table records no clinical significance for this variant.
Reference-table entries
CBR3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 21:37507745
- HGVS
- NM_001236.4,c.255C>T,p.Asn85Asn
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.