List of variants in gene FLNB reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
NM_001457.4(FLNB):c.6684C>T (p.Ile2228=)	rs138416613	0.00170
NM_001457.4(FLNB):c.6642C>T (p.Phe2214=)	rs140786324	0.00161
NM_001457.4(FLNB):c.6741G>A (p.Ser2247=)	rs143400214	0.00141
NM_001457.4(FLNB):c.808A>G (p.Met270Val)	rs145036794	0.00096
NM_001457.4(FLNB):c.1203C>T (p.Thr401=)	rs148507053	0.00021

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