ClinVar Miner

List of variants reported as uncertain significance for Charcot-Marie-Tooth disease dominant intermediate B by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.1712A>G (p.Lys571Arg)	rs760694871	0.00001
NM_001005361.3(DNM2):c.70G>A (p.Gly24Ser)	rs2512931490
NM_001005361.3(DNM2):c.953G>A (p.Arg318Gln)	rs879254323

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