ClinVar Miner

List of variants in gene combination MED25, MIR6800 reported as benign for Charcot-Marie-Tooth disease type 2

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Minimum conflict level: Report conflict between different conditions
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_030973.4(MED25):c.1316+23del
NM_030973.4(MED25):c.1317-3del	rs2074062033

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