ClinVar Miner

List of variants in gene combination FLNC, LOC129999273 reported as likely benign for Cardiomyopathy

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.2128G>A (p.Asp710Asn)	rs370035829	0.00019
NM_001458.5(FLNC):c.2142C>A (p.Ile714=)	rs199595235

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