Variant (rsID / SNP)
rs10406069
rs10406069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD22. Location: chromosome 19, position 35,836,530. The table records no clinical significance for this variant.
Reference-table entries
CD22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:35836530
- HGVS
- NM_001771.4,c.2234G>A,p.Gly745Asp
- Allele change
- Missense_G573D
Associated conditions / phenotypes
Childhood Acute Lymphocytic Leukemia|Leukemia|Leukemia, Acute Lymphoblastic|Scleroderma, Familial Progressive
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.