List of variants in gene combination FBN1, LOC126862124 reported as benign for Marfan syndrome; Familial thoracic aortic aneurysm and aortic dissection

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.4211-10C>T	rs28730793	0.00006
NM_000138.5(FBN1):c.4316C>G (p.Ala1439Gly)	rs755085498	0.00005
NM_000138.5(FBN1):c.4306G>A (p.Val1436Met)	rs377338217	0.00001

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