Variant (rsID / SNP)
rs2072671
rs2072671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDA. Location: chromosome 1, position 20,915,701. The table records no clinical significance for this variant.
Reference-table entries
CDANot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:20915701
- HGVS
- NM_001785.3,c.79A>C,p.Lys27Gln
- Allele change
- Missense_K27Q
Associated conditions / phenotypes
Leukemia, Acute Myeloid|Neutropenia|Pancreatic Cancer|Thrombocytopenia|Myeloid Leukemia|Mucositis|Chronic Myelomonocytic Leukemia|Leukemia|Myelodysplastic Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.