List of variants in gene FBN2 reported as likely 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001999.4(FBN2):c.5675-9C>T	rs27713	0.68788
NM_001999.4(FBN2):c.111G>A (p.Pro37=)	rs55715053	0.14249
NM_001999.4(FBN2):c.183C>G (p.Pro61=)	rs73348287	0.10581
NM_001999.4(FBN2):c.203C>T (p.Ala68Val)	rs62390671	0.03303
NM_001999.4(FBN2):c.4098A>C (p.Thr1366=)	rs28763943	0.02427
NM_001999.4(FBN2):c.2778C>T (p.Ala926=)	rs28763948	0.00992
NM_001999.4(FBN2):c.1466-5C>T	rs28763952	0.00887
NM_001999.4(FBN2):c.8154C>T (p.Leu2718=)	rs34119447	0.00635
NM_001999.4(FBN2):c.629-9A>G	rs56025995	0.00616
NM_001999.4(FBN2):c.8347G>C (p.Glu2783Gln)	rs76756898	0.00599
NM_001999.4(FBN2):c.1040G>A (p.Arg347His)	rs112428886	0.00427
NM_001999.4(FBN2):c.7181T>C (p.Ile2394Thr)	rs28763926	0.00287
NM_001999.4(FBN2):c.4206C>T (p.Asn1402=)	rs34201226	0.00261
NM_001999.4(FBN2):c.829G>A (p.Val277Ile)	rs146849637	0.00210
NM_001999.4(FBN2):c.1961G>C (p.Arg654Pro)	rs780589159
NM_001999.4(FBN2):c.2161G>A (p.Gly721Ser)	rs149733159
NM_001999.4(FBN2):c.6948C>A (p.Ile2316=)	rs17608368

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