Variant (rsID / SNP)
rs769784756
rs769784756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDC73. Location: chromosome 1, position 193,205,495. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CDC73Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:193205495
- Cytoband
- 1q31.2
- HGVS
- NM_024529.5(CDC73):c.1417+9C>T
- Allele change
- Silent
Associated conditions / phenotypes
Hyperparathyroidism 2 with jaw tumors|Hyperparathyroidism 1|Parathyroid carcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.