List of variants in gene combination LMNA, LOC126805877 reported as likely pathogenic for Primary dilated cardiomyopathy

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.448A>G (p.Thr150Ala)	rs58917027	0.00001
NM_170707.4(LMNA):c.364AAG[1] (p.Lys123del)	rs794728597
NM_170707.4(LMNA):c.448A>C (p.Thr150Pro)	rs58917027
NM_170707.4(LMNA):c.476del (p.Glu159fs)	rs876657650
NM_170707.4(LMNA):c.485T>C (p.Leu162Pro)	rs267607594
NM_170707.4(LMNA):c.497G>C (p.Arg166Pro)	rs267607570
NM_170707.4(LMNA):c.513+1G>C	rs397517904

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