Variant (rsID / SNP)
rs1883832
rs1883832 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD40. Location: chromosome 20, position 44,746,982. Clinical significance in the table: Benign.
Reference-table entries
CD40Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 20:44746982
- Cytoband
- 20q13.12
- HGVS
- NM_001250.6(CD40):c.-1T>C
- Allele change
- Silent
Associated conditions / phenotypes
Hyper-IgM syndrome type 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.