List of variants in gene combination LMNA, LOC126805877 reported as likely benign for 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.471G>A (p.Thr157=)	rs150645079	0.00008
NM_170707.4(LMNA):c.357-8T>C	rs1053291240	0.00004
NM_170707.4(LMNA):c.357-13C>A	rs1264489096	0.00001
NM_170707.4(LMNA):c.357-15C>T	rs779619961	0.00001
NM_170707.4(LMNA):c.369G>A (p.Lys123=)	rs367938270	0.00001
NM_170707.4(LMNA):c.480C>A (p.Gly160=)	rs758848135	0.00001
NM_170707.4(LMNA):c.375T>C (p.Gly125=)	rs1164862537
NM_170707.4(LMNA):c.486G>A (p.Leu162=)	rs727503135
NM_170707.4(LMNA):c.513+8del	rs1650992817

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