ClinVar Miner

List of variants in gene combination LMNA, LOC126805877 reported as benign for Charcot-Marie-Tooth disease type 2

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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_170707.4(LMNA):c.438C>T (p.Ala146=)	rs80356805	0.00738
NM_170707.4(LMNA):c.357C>T (p.Arg119=)	rs41313880	0.00321

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