List of variants reported as likely benign for B cell deficiency by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006846.4(SPINK5):c.2243A>G (p.Glu748Gly)	rs181639116	0.00297
NM_052945.4(TNFRSF13C):c.317G>A (p.Arg106Gln)	rs150374940	0.00202
NM_080911.3(UNG):c.533+6G>A	rs55812333	0.00163
NM_139276.3(STAT3):c.1329C>T (p.Thr443=)	rs147955721	0.00091

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