List of variants in gene FBN2 reported as pathogenic for not provided

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.3472+2T>C	rs2126903614
NM_001999.4(FBN2):c.3724+2T>C	rs863223570
NM_001999.4(FBN2):c.4222+5G>A	rs1554122550
NM_001999.4(FBN2):c.4274G>A (p.Cys1425Tyr)
NM_001999.4(FBN2):c.525T>A (p.Cys175Ter)	rs863223547
NM_001999.4(FBN2):c.5801-633_6166+1908del

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