Variant (rsID / SNP)

rs2070776

rs2070776 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD79B. Location: chromosome 17, position 62,007,498. Clinical significance in the table: Benign.

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Reference-table entries

CD79BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:62007498
Cytoband: 17q23.3
HGVS: NM_000626.4(CD79B):c.366T>C (p.Cys122=)
Allele change: Silent

Associated conditions / phenotypes

Agammaglobulinemia 6, autosomal recessive

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.