List of variants in gene PMPCB reported as likely benign by Ambry Genetics

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_004279.3(PMPCB):c.1336A>G (p.Asn446Asp)	rs144744182	0.00172
NM_004279.3(PMPCB):c.838A>T (p.Thr280Ser)	rs145484475	0.00013
NM_004279.3(PMPCB):c.1348A>G (p.Ile450Val)	rs1817776297	0.00001

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