Variant (rsID / SNP)
rs11891
rs11891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CANT1. Location: chromosome 17, position 76,988,785. Clinical significance in the table: Benign.
Reference-table entries
CANT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:76988785
- Cytoband
- 17q25.3
- HGVS
- NM_001159773.2(CANT1):c.*847C>T
- Allele change
- Silent
Associated conditions / phenotypes
Desbuquois dysplasia 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.