Variant (rsID / SNP)
rs1005696
rs1005696 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBR1-AS1, CBR1. Location: chromosome 21, position 37,443,480. The table records no clinical significance for this variant.
Reference-table entries
CBR1-AS1Not classified
- Variant type
- intron_variant
- Chromosome / position
- 21:37443480
- HGVS
- NR_040084.1,n.378-697A>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.