List of variants in gene CHMP2B reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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_014043.4(CHMP2B):c.312T>C (p.Thr104=)	rs11540913	0.83212
NM_014043.4(CHMP2B):c.27C>T (p.Thr9=)	rs2279720	0.09131
NM_014043.4(CHMP2B):c.372A>C (p.Thr124=)	rs1044499	0.09006

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