ClinVar Miner

List of variants reported as benign for immunodeficiency due to a late component of complement deficiency by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (10):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000065.5(C6):c.1881C>T (p.Asp627=)	rs6866352	0.99985
NM_000562.3(C8A):c.107C>A (p.Ala36Glu)	rs116201358

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