List of variants in gene LMNA reported as benign 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1338T>C (p.Asp446=)	rs505058	0.22862
NM_170707.4(LMNA):c.1698C>T (p.His566=)	rs4641	0.20715
NM_170707.4(LMNA):c.861T>C (p.Ala287=)	rs538089	0.18331
NM_170707.4(LMNA):c.1157+16G>A	rs534807	0.17703
NM_170707.4(LMNA):c.810+13G>T	rs11264444	0.05317
NM_170707.4(LMNA):c.612G>A (p.Leu204=)	rs12117552	0.00637
NM_170707.4(LMNA):c.1761G>A (p.Leu587=)	rs80356813	0.00210
NM_170707.4(LMNA):c.1851C>T (p.Ala617=)	rs143189394	0.00158
NM_170707.4(LMNA):c.1911C>T (p.Phe637=)	rs117939448	0.00048
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_005572.4(LMNA):c.1712G>A (p.Arg571His)	rs200917748	0.00003

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