List of variants in gene LMNA reported as benign by Athena Diagnostics Inc

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: 10

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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.612G>A (p.Leu204=)	rs12117552	0.00637
NM_170707.4(LMNA):c.1761G>A (p.Leu587=)	rs80356813	0.00210
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.895A>G (p.Ile299Val)	rs150924946	0.00016
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035

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