Variants in gene FLNC with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.4871C>T (p.Ser1624Leu)	rs879255639	0.00003
NM_001458.5(FLNC):c.4636G>A (p.Gly1546Ser)	rs774263134	0.00002
NM_001458.5(FLNC):c.3791-1G>C	rs781135153	0.00001
NM_001458.5(FLNC):c.1948C>T (p.Arg650Ter)	rs770606675
NM_001458.5(FLNC):c.2838T>A (p.Tyr946Ter)	rs769390195
NM_001458.5(FLNC):c.2971C>T (p.Arg991Ter)	rs886037830
NM_001458.5(FLNC):c.3180del (p.Asp1061fs)	rs1064795229
NM_001458.5(FLNC):c.3934_3937dup (p.Arg1313fs)	rs1554399513
NM_001458.5(FLNC):c.3937C>T (p.Arg1313Ter)	rs766330686
NM_001458.5(FLNC):c.4021C>T (p.Arg1341Ter)	rs1562998062
NM_001458.5(FLNC):c.4456+1G>A	rs1318885805
NM_001458.5(FLNC):c.4621A>T (p.Lys1541Ter)	rs1562999451
NM_001458.5(FLNC):c.4926_4927insACGTCACA (p.Val1643fs)	rs1402879259
NM_001458.5(FLNC):c.4969C>T (p.Arg1657Ter)	rs1563000044
NM_001458.5(FLNC):c.577G>A (p.Ala193Thr)	rs387906587
NM_001458.5(FLNC):c.6190dup (p.Val2064fs)	rs1808888920
NM_001458.5(FLNC):c.6864_6867dup (p.Val2290fs)	rs2128939508

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