Gene entry
CDKN1B
cyclin dependent kinase inhibitor 1B
- Chromosome
- 12
- Cytoband
- 12p13.1
- Variants (rsID)
- 12
CDKN1B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p13.1). Its official name is “cyclin dependent kinase inhibitor 1B”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
12 reference-table entries with clinical significance.
- rs2066827Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Multiple endocrine neoplasia type 4
- rs34330Benignsingle nucleotide variantMultiple endocrine neoplasia type 4
- rs73281150Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Multiple endocrine neoplasia type 4
- rs137985549Conflicting interpretationssingle nucleotide variantMultiple endocrine neoplasia type 4|Primary hyperparathyroidism|Hereditary cancer-predisposing syndrome
- rs139727620Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Multiple endocrine neoplasia type 4
- rs140167393Conflicting interpretationssingle nucleotide variantMultiple endocrine neoplasia type 4|Hereditary cancer-predisposing syndrome
- rs142833529Conflicting interpretationssingle nucleotide variantMultiple endocrine neoplasia type 4|Hereditary cancer-predisposing syndrome
- rs373917399Conflicting interpretationssingle nucleotide variantMultiple endocrine neoplasia type 4|Hereditary cancer-predisposing syndrome
- rs546234840Conflicting interpretationssingle nucleotide variantMultiple endocrine neoplasia type 4|Hereditary cancer-predisposing syndrome
- rs774454456Conflicting interpretationsMicrosatelliteMultiple endocrine neoplasia type 4|Primary hyperparathyroidism|Multiple endocrine neoplasia
- rs200422211Uncertain significancesingle nucleotide variantMultiple endocrine neoplasia type 4|Hereditary cancer-predisposing syndrome
- rs200476090Uncertain significancesingle nucleotide variantMultiple endocrine neoplasia type 4
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.