List of variants in gene FBN2 reported as not provided for arthrogryposis syndrome

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001999.4(FBN2):c.8530G>A (p.Val2844Ile)	rs147134796	0.00007
NM_001999.4(FBN2):c.3805A>G (p.Ser1269Gly)	rs765649978	0.00004
NM_001999.4(FBN2):c.2773G>A (p.Gly925Arg)	rs111405756
NM_001999.4(FBN2):c.4244G>T (p.Gly1415Val)	rs2126889179
NM_001999.4(FBN2):c.4346-2A>T	rs587776518
NM_001999.4(FBN2):c.8082C>A (p.His2694Gln)	rs142755118

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