ClinVar Miner

List of variants in gene combination DNM2, LOC130063529, MIR638 reported as uncertain significance for Charcot-Marie-Tooth disease dominant intermediate B

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001005361.3(DNM2):c.161+6C>T	rs2068821980	0.00001
NM_001005361.3(DNM2):c.161+3G>A	rs1555696272

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