Variants in gene PMP22 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_000304.4(PMP22):c.353C>T (p.Thr118Met)	rs104894619	0.00378
NM_000304.4(PMP22):c.233T>C (p.Leu78Pro)	rs1555565276
NM_000304.4(PMP22):c.341C>T (p.Ala114Val)	rs1217342392
NM_000304.4(PMP22):c.392C>G (p.Ser131Cys)	rs1597597627
NM_000304.4(PMP22):c.68C>G (p.Thr23Arg)	rs906563423

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