List of variants reported as uncertain significance for agammaglobulinemia 8b, autosomal recessive by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_003200.5(TCF3):c.1430G>A (p.Arg477Gln)	rs199957863	0.00012
NM_003200.5(TCF3):c.23C>T (p.Ala8Val)	rs376780559	0.00008
NM_001136139.4(TCF3):c.1732A>G (p.Lys578Glu)	rs752741173	0.00001
NM_003200.5(TCF3):c.955+3A>G	rs774512132	0.00001
NM_003200.5(TCF3):c.217C>T (p.Arg73Trp)
NM_003200.5(TCF3):c.555C>A (p.Tyr185Ter)
NM_003200.5(TCF3):c.730T>C (p.Ser244Pro)
NM_003200.5(TCF3):c.853G>A (p.Gly285Ser)

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