List of variants in gene LMNA studied for Laminopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1045C>T (p.Arg349Trp)	rs267607555	0.00001
NM_170707.4(LMNA):c.1445G>A (p.Arg482Gln)	rs11575937	0.00001
NM_005572.4(LMNA):c.1711C>A (p.Arg571Ser)	rs80338938
NM_170707.4(LMNA):c.1110C>G (p.Asp370Glu)	rs876657649
NM_170707.4(LMNA):c.1621C>T (p.Arg541Cys)	rs56984562
NM_170707.4(LMNA):c.745C>G (p.Arg249Gly)	rs121912496

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