Variant (rsID / SNP)
rs35112940
rs35112940 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD33. Location: chromosome 19, position 51,738,917. The table records no clinical significance for this variant.
Reference-table entries
CD33Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:51738917
- HGVS
- NM_001772.4,c.910G>A,p.Gly304Arg
- Allele change
- Missense_G304R
Associated conditions / phenotypes
Leukemia, Acute Myeloid|Myeloid Leukemia|Childhood Acute Myeloid Leukemia|Leukemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.