List of variants in gene FLNC reported as uncertain significance by Institute of Human Genetics, University of Wuerzburg

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.352+3C>T	rs750255204	0.00001
NM_001458.5(FLNC):c.7280C>T (p.Ala2427Val)	rs1343869103	0.00001
NM_001458.5(FLNC):c.1325C>G (p.Pro442Arg)	rs1554397822
NM_001458.5(FLNC):c.308C>A (p.Ala103Asp)
NM_001458.5(FLNC):c.3275_3278delinsAAGA (p.Thr1092_Gly1093delinsLysAsp)	rs1585159928
NM_001458.5(FLNC):c.4192A>G (p.Lys1398Glu)	rs1585162066
NM_001458.5(FLNC):c.4345T>C (p.Ser1449Pro)
NM_001458.5(FLNC):c.4425G>T (p.Ala1475=)
NM_001458.5(FLNC):c.6429G>T (p.Gln2143His)

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