List of variants in gene combination LOC129999056, PMPCB reported as benign

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.-23C>T	rs2301861	0.01018
NM_004279.3(PMPCB):c.99+115C>T	rs192846145	0.00919
NM_004279.3(PMPCB):c.8C>T (p.Ala3Val)	rs138251541	0.00233

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