List of variants reported as uncertain significance for B cell deficiency by Department of Human Genetics, Hannover Medical School

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001364905.1(LRBA):c.1931C>T (p.Pro644Leu)	rs371718439	0.00007
NM_181523.3(PIK3R1):c.347C>T (p.Pro116Leu)	rs774531250	0.00004
NM_001364905.1(LRBA):c.7085A>G (p.Asn2362Ser)
NM_012452.3(TNFRSF13B):c.446-3C>A

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