List of variants in gene CR2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001006658.3(CR2):c.2611G>T (p.Val871Leu)	rs144572703	0.00319
NM_001006658.3(CR2):c.2844G>A (p.Glu948=)	rs61754518	0.00098
NM_001006658.3(CR2):c.2646T>C (p.Asn882=)	rs1658400318
NM_001006658.3(CR2):c.3189-8_3189-7del	rs112859639
NM_001006658.3(CR2):c.524C>T (p.Pro175Leu)	rs75282758

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