List of variants in gene FBN1 reported as likely benign by Eurofins NTD LLC (GA)

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.8502T>C (p.Thr2834=)	rs363847	0.00148
NM_000138.5(FBN1):c.7950T>C (p.Asn2650=)	rs143055643	0.00113
NM_000138.5(FBN1):c.6681A>C (p.Ser2227=)	rs363824	0.00109
NM_000138.5(FBN1):c.2956G>A (p.Ala986Thr)	rs112287730	0.00107
NM_000138.5(FBN1):c.6837G>A (p.Gly2279=)	rs140584234	0.00094
NM_000138.5(FBN1):c.783T>C (p.Asn261=)	rs113721547	0.00091
NM_000138.5(FBN1):c.2892C>T (p.Asp964=)	rs116945525	0.00010

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