"GeneDx"[submitter] AND "C1QC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1167797	NM_172369.5(C1QC):c.126C>T (p.Pro42=)	C1QC	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1251622	NM_172369.5(C1QC):c.181+93A>T	C1QC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280557	NM_172369.5(C1QC):c.181+131G>T	C1QC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232024	NM_172369.5(C1QC):c.181+211C>T	C1QC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260388	NM_172369.5(C1QC):c.181+228T>C	C1QC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251013	NM_172369.5(C1QC):c.182-21C>G	C1QC	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221376	NM_172369.5(C1QC):c.*21C>A	C1QC	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1257095	NM_172369.5(C1QC):c.272_273del	C1QC	Deletion (3 prime UTR variant)	not provided	GBenign

ClinVar