List of variants in gene CR2 reported as likely benign for not provided

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: 17

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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.2352T>C (p.Ile784=)	rs142319454	0.00170
NM_001006658.3(CR2):c.1458T>C (p.Phe486=)	rs147378770	0.00115
NM_001006658.3(CR2):c.2628T>G (p.Asn876Lys)	rs138979306	0.00113
NM_001006658.3(CR2):c.2844G>A (p.Glu948=)	rs61754518	0.00098
NM_001006658.3(CR2):c.2747C>T (p.Thr916Ile)	rs61754517	0.00033
NM_001006658.3(CR2):c.276T>G (p.Pro92=)	rs371546344	0.00006
NM_001006658.3(CR2):c.21C>T (p.Leu7=)	rs779365020	0.00005
NM_001006658.3(CR2):c.621C>T (p.Pro207=)	rs573346582	0.00003
NM_001006658.3(CR2):c.3261A>G (p.Pro1087=)	rs374978382	0.00001
NM_001006658.3(CR2):c.2225C>T (p.Thr742Met)
NM_001006658.3(CR2):c.2646T>C (p.Asn882=)	rs1658400318
NM_001006658.3(CR2):c.2688G>T (p.Val896=)	rs1250358980
NM_001006658.3(CR2):c.3189-8_3189-7del	rs112859639
NM_001006658.3(CR2):c.524C>T (p.Pro175Leu)	rs75282758
NM_001006658.3(CR2):c.624C>A (p.Pro208=)	rs61759494
NM_001006658.3(CR2):c.9C>T (p.Ala3=)

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