List of variants in gene CORO2B 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006091.5(CORO2B):c.581T>A (p.Leu194Gln)	rs138122643	0.00253
NM_006091.5(CORO2B):c.186C>T (p.Gly62=)	rs61747072	0.00131
NM_006091.5(CORO2B):c.540G>A (p.Thr180=)	rs144633179	0.00027

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