List of variants in gene LMNA reported as 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1338T>C (p.Asp446=)	rs505058	0.23806
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	0.18318
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.811-13T>A	rs80356809	0.00309
NM_005572.3(LMNA):c.-223C>T	rs188625872	0.00284
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.1566C>T (p.Cys522=)	rs149339264	0.00123
NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys)	rs142000963	0.00117
NM_170707.4(LMNA):c.1911C>T (p.Phe637=)	rs117939448	0.00048
NM_170707.4(LMNA):c.789G>A (p.Leu263=)	rs148557956	0.00048
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_170707.4(LMNA):c.1017G>A (p.Ala339=)	rs17847242	0.00021
NM_170707.4(LMNA):c.1488+14C>T	rs377700689	0.00013
NM_170707.4(LMNA):c.1149G>A (p.Glu383=)	rs267607603	0.00006
NM_005572.4(LMNA):c.1712G>A (p.Arg571His)	rs200917748	0.00003
NM_170707.4(LMNA):c.1227A>G (p.Thr409=)	rs762130433	0.00003
NM_170707.4(LMNA):c.1324G>A (p.Val442Met)	rs368542816	0.00003
NM_170707.4(LMNA):c.948G>A (p.Lys316=)	rs778421025	0.00001
NM_170707.4(LMNA):c.-88G>T	rs115800510
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035
NM_170707.4(LMNA):c.572T>G (p.Val191Gly)	rs752087253

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