List of variants in gene combination LMNA, LOC126805877 reported as uncertain significance for Cardiomyopathy

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.497G>A (p.Arg166Gln)	rs267607570	0.00005
NM_170707.4(LMNA):c.467G>A (p.Arg156His)	rs764475194	0.00004
NM_170707.4(LMNA):c.364A>G (p.Lys122Glu)	rs1222398892	0.00002
NM_170707.4(LMNA):c.398G>A (p.Arg133Gln)	rs60864230	0.00001
NM_170707.4(LMNA):c.451G>A (p.Ala151Thr)	rs766291714	0.00001
NM_170707.4(LMNA):c.478G>C (p.Gly160Arg)	rs765665953	0.00001
NM_170707.4(LMNA):c.480C>T (p.Gly160=)	rs758848135	0.00001
NM_170707.4(LMNA):c.496C>T (p.Arg166Trp)	rs370200334	0.00001
NM_170707.4(LMNA):c.370G>A (p.Glu124Lys)	rs2102865393
NM_170707.4(LMNA):c.373G>A (p.Gly125Ser)	rs267607605
NM_170707.4(LMNA):c.379C>T (p.Leu127=)	rs1428192739
NM_170707.4(LMNA):c.382A>G (p.Ile128Val)	rs1338283666
NM_170707.4(LMNA):c.383T>C (p.Ile128Thr)	rs746475627
NM_170707.4(LMNA):c.386C>A (p.Ala129Asp)	rs768203943
NM_170707.4(LMNA):c.470C>A (p.Thr157Lys)	rs754097769
NM_170707.4(LMNA):c.488A>G (p.His163Arg)	rs1650987918
NM_170707.4(LMNA):c.489T>G (p.His163Gln)	rs1558126350
NM_170707.4(LMNA):c.503A>G (p.Gln168Arg)	rs1371187616
NM_170707.4(LMNA):c.511A>G (p.Lys171Glu)	rs1650991296

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