List of variants in gene FLNB reported as likely benign by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.4222+8A>G	rs190025781	0.00248
NM_001457.4(FLNB):c.1559C>T (p.Pro520Leu)	rs138220431	0.00247
NM_001457.4(FLNB):c.1472T>C (p.Met491Thr)	rs147575358	0.00203
NM_001457.4(FLNB):c.6231C>T (p.Asp2077=)	rs145280904	0.00184
NM_001457.4(FLNB):c.6683T>C (p.Ile2228Thr)	rs149629209	0.00148
NM_001457.4(FLNB):c.4929C>T (p.Ala1643=)	rs149070858	0.00140
NM_001457.4(FLNB):c.5445C>T (p.Tyr1815=)	rs755702006	0.00019
NM_001457.4(FLNB):c.5769C>T (p.Ala1923=)	rs201723447	0.00019
NM_001457.4(FLNB):c.4390+8T>A	rs377095569	0.00018
NM_001457.4(FLNB):c.2773G>T (p.Gly925Cys)	rs139875974
NM_001457.4(FLNB):c.4515-24GT[4]	rs151085835

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