ClinVar Miner

List of variants reported as likely benign for Hyper-IgM syndrome type 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_020661.4(AICDA):c.74G>A (p.Arg25His) rs61730095 0.00289

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