ClinVar Miner

List of variants reported as likely benign for C1Q deficiency by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_015991.4(C1QA):c.67G>A (p.Glu23Lys)	rs17887074	0.00330
NM_001378156.1(C1QB):c.543C>T (p.Asn181=)	rs149612866	0.00265

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