List of variants in gene LMNA reported as likely pathogenic for Muscular dystrophy

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1147GAG[2] (p.Glu385del)	rs1553265761
NM_170707.4(LMNA):c.1163G>C (p.Arg388Pro)	rs267607576
NM_170707.4(LMNA):c.790_792del (p.Glu264del)	rs1553265369

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