Variants in gene PMP22 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000304.4(PMP22):c.*228G>A	rs1804193	0.05698
NM_000304.4(PMP22):c.353C>T (p.Thr118Met)	rs104894619	0.00378
NM_000304.4(PMP22):c.403G>A (p.Ala135Thr)	rs141094419	0.00278
NM_000304.4(PMP22):c.178+7C>A	rs147885521	0.00111
NM_000304.4(PMP22):c.-6G>T	rs369779295	0.00103
NM_000304.4(PMP22):c.79-6C>T	rs201682989	0.00086

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