ClinVar Miner

List of variants in gene FCN3 reported as likely benign for Immunodeficiency due to ficolin3 deficiency

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003665.4(FCN3):c.750C>T (p.His250=)	rs28385652	0.00249
NM_003665.4(FCN3):c.498G>C (p.Glu166Asp)	rs56405086	0.00087

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