List of variants in gene combination LOC130064454, PRX reported as uncertain significance for Charcot-Marie-Tooth disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_181882.3(PRX):c.133C>G (p.Arg45Gly)	rs115090201	0.00569
NM_181882.3(PRX):c.116_117del (p.Lys39fs)	rs1599662861
NM_181882.3(PRX):c.145G>T (p.Glu49Ter)	rs1024162447
NM_181882.3(PRX):c.158C>A (p.Ala53Asp)	rs753322071
NM_181882.3(PRX):c.44A>G (p.Glu15Gly)	rs202192239

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