List of variants in gene LMNA reported as pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.992G>A (p.Arg331Gln)	rs59301204	0.00004
NM_170707.4(LMNA):c.1003C>T (p.Arg335Trp)	rs386134243	0.00001
NM_170707.4(LMNA):c.646C>T (p.Arg216Cys)	rs794728591	0.00001
NM_170707.4(LMNA):c.949G>A (p.Glu317Lys)	rs56816490	0.00001
NM_170707.4(LMNA):c.1072G>A (p.Glu358Lys)	rs60458016
NM_170707.4(LMNA):c.1158-1G>A
NM_170707.4(LMNA):c.1233del (p.Gly413fs)
NM_170707.4(LMNA):c.184C>G (p.Arg62Gly)	rs56793579
NM_170707.4(LMNA):c.1961dup (p.Thr655fs)	rs863225024
NM_170707.4(LMNA):c.569G>A (p.Arg190Gln)	rs267607571
NM_170707.4(LMNA):c.711_729delinsCC (p.Glu238fs)	rs1572359848
NM_170707.4(LMNA):c.746G>A (p.Arg249Gln)	rs59332535
NM_170707.4(LMNA):c.961C>T (p.Arg321Ter)	rs267607554

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