Variant (rsID / SNP)
rs1048977
rs1048977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDA. Location: chromosome 1, position 20,945,055. The table records no clinical significance for this variant.
Reference-table entries
CDANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:20945055
- HGVS
- NM_001785.3,c.435C>T,p.Thr145Thr
- Allele change
- Synonymous_T145T
Associated conditions / phenotypes
Myeloid Leukemia|Biliary Tract Cancer
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.