Variant (rsID / SNP)

rs144367487

rs144367487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD79A. Location: chromosome 19, position 42,383,351. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CD79AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:42383351
Cytoband: 19q13.2
HGVS: NM_001783.4(CD79A):c.371G>A (p.Arg124His)
Allele change: Silent

Associated conditions / phenotypes

Agammaglobulinemia 3, 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.