Variant (rsID / SNP)
rs11907350
rs11907350 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP24A1. Location: chromosome 20, position 52,770,439. Clinical significance in the table: Benign.
Reference-table entries
CYP24A1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:52770439
- Cytoband
- 20q13.2
- HGVS
- NM_000782.5(CYP24A1):c.*872C>T
- Allele change
- Silent
Associated conditions / phenotypes
Hypercalcemia, infantile, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.