List of variants reported as benign for Marfan syndrome by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.3442C>G (p.Pro1148Ala)	rs140598	0.01315
NM_000138.5(FBN1):c.3965-8T>C	rs140637	0.00859
NM_000138.5(FBN1):c.986T>C (p.Ile329Thr)	rs12324002	0.00737
NM_000138.5(FBN1):c.6594C>T (p.Pro2198=)	rs111844882	0.00439
NM_000138.5(FBN1):c.1746C>T (p.Cys582=)	rs112366266	0.00436
NM_000138.5(FBN1):c.3675G>A (p.Pro1225=)	rs148147223	0.00436
NM_000138.5(FBN1):c.4905C>G (p.Thr1635=)	rs113115949	0.00435
NM_000138.5(FBN1):c.3082+8del	rs193922196	0.00359
NM_000138.5(FBN1):c.2055C>T (p.Cys685=)	rs140603	0.00304
NM_000138.5(FBN1):c.8502T>C (p.Thr2834=)	rs363847	0.00148
NM_000138.5(FBN1):c.6073G>T (p.Ala2025Ser)	rs113577372	0.00115
NM_000138.5(FBN1):c.2956G>A (p.Ala986Thr)	rs112287730	0.00107
NM_000138.5(FBN1):c.6700G>A (p.Val2234Met)	rs112084407	0.00078
NM_000138.5(FBN1):c.510C>T (p.Tyr170=)	rs111671429	0.00076
NM_000138.5(FBN1):c.6832C>T (p.Pro2278Ser)	rs363835

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