List of variants reported as uncertain significance for Immunodeficiency due to ficolin3 deficiency

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_003665.4(FCN3):c.232+1G>A	rs141300199	0.00153
NM_003665.4(FCN3):c.620A>G (p.Tyr207Cys)	rs781053078	0.00002
NM_003665.4(FCN3):c.142G>A (p.Gly48Arg)
NM_003665.4(FCN3):c.349del (p.Leu117fs)	rs532781899
NM_003665.4(FCN3):c.440G>T (p.Trp147Leu)
NM_003665.4(FCN3):c.797G>A (p.Arg266His)

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