List of variants in gene PMP22 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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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.255C>G (p.Cys85Trp)	rs755701957	0.00002
NM_000304.4(PMP22):c.407A>C (p.Tyr136Ser)	rs375449671	0.00002
NM_000304.4(PMP22):c.74T>G (p.Val25Gly)	rs765741053	0.00001
NM_000304.4(PMP22):c.281del (p.Gly94fs)	rs80338763
NM_000304.4(PMP22):c.396C>A (p.Tyr132Ter)
Single allele

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