List of variants in gene combination LMNA, LOC126805877 reported as pathogenic for laminopathy

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.398G>C (p.Arg133Pro)	rs60864230
NM_170707.4(LMNA):c.398G>T (p.Arg133Leu)	rs60864230
NM_170707.4(LMNA):c.513+45T>G	rs878853220

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