List of variants in gene FLNB reported as likely pathogenic for atelosteogenesis

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.1739G>T (p.Gly580Val)	rs2097257677
NM_001457.4(FLNB):c.641TCA[1] (p.Ile215del)
NM_001457.4(FLNB):c.644T>A (p.Ile215Asn)	rs2097209399

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