List of variants in gene FBN2 reported as benign for perceptual disorders

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: 7

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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.5675-9C>T	rs27713	0.68788
NM_001999.4(FBN2):c.2893G>A (p.Val965Ile)	rs154001	0.68054
NM_001999.4(FBN2):c.6880+17G>A	rs2042327	0.45423
NM_001999.4(FBN2):c.1466-5C>T	rs28763952	0.00887
NM_001999.4(FBN2):c.5353+19C>T	rs183524866	0.00179
NM_001999.4(FBN2):c.3848-10G>T	rs140017238

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