ClinVar Miner

List of variants reported as uncertain significance for agammaglobulinemia 3, autosomal recessive by Invitae

Included ClinVar conditions (1):
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Total variants: 9
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HGVS dbSNP
NM_001783.3(CD79A):c.188A>G (p.Asn63Ser)
NM_001783.3(CD79A):c.224C>A (p.Thr75Lys)
NM_001783.3(CD79A):c.258C>A (p.Asp86Glu) rs587778166
NM_001783.3(CD79A):c.269C>T (p.Thr90Met)
NM_001783.3(CD79A):c.370C>T (p.Arg124Cys) rs144006380
NM_001783.3(CD79A):c.371G>A (p.Arg124His) rs144367487
NM_001783.3(CD79A):c.502C>G (p.Arg168Gly) rs1555844064
NM_001783.3(CD79A):c.593T>C (p.Met198Thr) rs532288711
NM_001783.3(CD79A):c.64T>A (p.Ser22Thr)

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