List of variants in gene LMNA reported as benign for Charcot-Marie-Tooth disease

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: 9

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HGVS	dbSNP
NM_170707.4(LMNA):c.1157+16G>A	rs534807
NM_170707.4(LMNA):c.1338T>C (p.Asp446=)	rs505058
NM_170707.4(LMNA):c.1698C>T (p.His566=)	rs4641
NM_170707.4(LMNA):c.357C>T (p.Arg119=)	rs41313880
NM_170707.4(LMNA):c.51C>T (p.Ser17=)	rs11549668
NM_170707.4(LMNA):c.612G>A (p.Leu204=)	rs12117552
NM_170707.4(LMNA):c.810+13G>T	rs11264444
NM_170707.4(LMNA):c.811-13T>A	rs80356809
NM_170707.4(LMNA):c.861T>C (p.Ala287=)	rs538089

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