List of variants in gene combination LMNA, LOC129931597 reported as likely pathogenic 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)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.104T>C (p.Leu35Pro)	rs267607644
NM_170707.4(LMNA):c.28A>C (p.Thr10Pro)
NM_170707.4(LMNA):c.28A>T (p.Thr10Ser)
NM_170707.4(LMNA):c.29C>G (p.Thr10Ser)
NM_170707.4(LMNA):c.73C>T (p.Arg25Cys)	rs58327533
NM_170707.4(LMNA):c.74G>A (p.Arg25His)
NM_170707.4(LMNA):c.74G>C (p.Arg25Pro)	rs61578124
NM_170707.4(LMNA):c.80C>T (p.Thr27Ile)	rs863225270

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