List of variants in gene LMNA reported as pathogenic for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
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)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP
NM_170707.4(LMNA):c.1411C>T (p.Arg471Cys)	rs28928902
NM_170707.4(LMNA):c.1444C>T (p.Arg482Trp)	rs57920071
NM_170707.4(LMNA):c.1579C>T (p.Arg527Cys)	rs57318642
NM_170707.4(LMNA):c.1580G>A (p.Arg527His)	rs57520892
NM_170707.4(LMNA):c.1908C>T (p.Ser636=)	rs80356814
NM_170707.4(LMNA):c.398G>T (p.Arg133Leu)	rs60864230
NM_170707.4(LMNA):c.892C>T (p.Arg298Cys)	rs59885338

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