List of variants in gene FBN2 reported as benign by Genetic Services Laboratory, University of Chicago

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001999.4(FBN2):c.7200T>C (p.Ser2400=)	rs190450	0.69111
NM_001999.4(FBN2):c.2893G>A (p.Val965Ile)	rs154001	0.68054
NM_001999.4(FBN2):c.8274C>T (p.Ser2758=)	rs10070365	0.13267
NM_001999.4(FBN2):c.6931A>G (p.Met2311Val)	rs32209	0.11103
NM_001999.4(FBN2):c.5823T>C (p.His1941=)	rs11955288	0.09446
NM_001999.4(FBN2):c.7739C>T (p.Ser2580Leu)	rs2291628	0.07011
NM_001999.4(FBN2):c.7013-5T>C	rs28763927	0.06995
NM_001999.4(FBN2):c.7296G>T (p.Gln2432His)	rs34600572	0.00870
NM_001999.4(FBN2):c.4312G>A (p.Glu1438Lys)	rs56168072	0.00832

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