ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease dominant intermediate B by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.2152C>T (p.Arg718Trp)	rs763927287	0.00001
NM_001005361.3(DNM2):c.2390C>T (p.Pro797Leu)	rs2073290117

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