"GenomeConnect - Invitae Patient Insights Network"[submitter] AND "CR2 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 571625	NM_001006658.3(CR2):c.668A>G (p.Asn223Ser)	CR2 (N223S)	Single nucleotide variant (missense variant)	Immunodeficiency, common variable, 7 +1 more	GUncertain significance
Select item 946072	NM_001006658.3(CR2):c.2018C>G (p.Thr673Arg)	CR2 (T673R)	Single nucleotide variant (missense variant +1 more)	Immunodeficiency, common variable, 7	GUncertain significance