List of variants in gene FBN2 reported as 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001999.4(FBN2):c.5675-9del	rs112666443	0.05000
NM_001999.4(FBN2):c.203C>T (p.Ala68Val)	rs62390671	0.03303
NM_001999.4(FBN2):c.728T>C (p.Ile243Thr)	rs117524265	0.00674
NM_001999.4(FBN2):c.976C>T (p.Pro326Ser)	rs28763954	0.00654
NM_001999.4(FBN2):c.629-9A>G	rs56025995	0.00616
NM_001999.4(FBN2):c.3762C>T (p.Asp1254=)	rs2279582	0.00570
NM_001999.4(FBN2):c.1040G>A (p.Arg347His)	rs112428886	0.00427
NM_001999.4(FBN2):c.5496C>T (p.Arg1832=)	rs35346129	0.00388
NM_001999.4(FBN2):c.6511+5G>A	rs200608284	0.00363
NM_001999.4(FBN2):c.2940C>T (p.Cys980=)	rs143255082	0.00158
NM_001999.4(FBN2):c.5448A>G (p.Pro1816=)	rs138022198	0.00158

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