ClinVar Miner

List of variants reported as benign for agammaglobulinemia 6, autosomal recessive

Included ClinVar conditions (1):
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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_000626.4(CD79B):c.366T>C (p.Cys122=) rs2070776 0.64196
NM_000626.4(CD79B):c.312C>T (p.Leu104=) rs116625909 0.00851
NM_000626.4(CD79B):c.118+12C>T rs150429226 0.00242
NM_000626.4(CD79B):c.550-17T>C rs199521114 0.00018
NM_000626.4(CD79B):c.550-8G>A rs202115514 0.00012
NM_000626.4(CD79B):c.102G>C (p.Arg34=) rs549278202
NM_000626.4(CD79B):c.549+11del rs750893342
NM_000626.4(CD79B):c.67+17G>C rs373437028

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