Variant (rsID / SNP)
rs4937076
rs4937076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDON. Location: chromosome 11, position 125,826,702. Clinical significance in the table: Benign.
Reference-table entries
CDONBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:125826702
- Cytoband
- 11q24.2
- HGVS
- NM_016952.4(CDON):c.*4135C>T
Associated conditions / phenotypes
Holoprosencephaly sequence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.