List of variants reported as uncertain significance for B cell deficiency by Clinical Genomics Laboratory, Washington University in St. Louis

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_012452.3(TNFRSF13B):c.61+5G>A	rs374249932	0.00005
NM_005026.5(PIK3CD):c.1607A>G (p.His536Arg)	rs1198694875	0.00003
NM_005026.5(PIK3CD):c.323G>T (p.Arg108Leu)	rs765031777	0.00003
NM_005026.5(PIK3CD):c.971G>A (p.Arg324His)	rs773473376	0.00002
NM_002184.4(IL6ST):c.2728G>C (p.Val910Leu)

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