Variant (rsID / SNP)
rs774454456
rs774454456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKN1B. Location: chromosome 12, position 12,870,745. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
CDKN1BConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- Microsatellite
- Chromosome / position
- 12:12870745
- Cytoband
- 12p13.1
- HGVS
- NM_004064.5(CDKN1B):c.-31AG[1]
Associated conditions / phenotypes
Multiple endocrine neoplasia type 4|Primary hyperparathyroidism|Multiple endocrine neoplasia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.