ClinVar Miner

List of variants in gene FLNB studied for See cases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001457.4(FLNB):c.3269A>G (p.Asn1090Ser)	rs755713308	0.00001
NM_001457.4(FLNB):c.1740dup (p.Ser581fs)	rs1000098671
NM_001457.4(FLNB):c.502G>A (p.Gly168Ser)	rs80356504

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