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

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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.497G>A (p.Arg166Gln)	rs267607570	0.00005
NM_170707.4(LMNA):c.467G>A (p.Arg156His)	rs764475194	0.00004
NM_170707.4(LMNA):c.398G>A (p.Arg133Gln)	rs60864230	0.00001
NM_170707.4(LMNA):c.466C>T (p.Arg156Cys)	rs760743233	0.00001
NM_170707.4(LMNA):c.496C>T (p.Arg166Trp)	rs370200334	0.00001
NM_170707.4(LMNA):c.365A>G (p.Lys122Arg)
NM_170707.4(LMNA):c.483G>A (p.Glu161=)	rs1553264647
NM_170707.4(LMNA):c.511A>G (p.Lys171Glu)	rs1650991296

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