ClinVar Miner

List of variants reported as likely benign for Severe combined immunodeficiency due to CARD11 deficiency; BENTA disease; Immunodeficiency 11b with atopic dermatitis by Fulgent Genetics, Fulgent Genetics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.1923G>A (p.Arg641=)	rs41405944	0.00786
NM_032415.7(CARD11):c.3454G>A (p.Asp1152Asn)	rs147422861	0.00217

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