List of variants in gene FLNC studied for Hypertrophic cardiomyopathy

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001458.5(FLNC):c.7947C>T (p.Phe2649=)	rs368849358	0.00083
NM_001458.5(FLNC):c.5954C>T (p.Ser1985Leu)	rs200415625	0.00031
NM_001458.5(FLNC):c.5296T>C (p.Trp1766Arg)	rs751650734	0.00015
NM_001458.5(FLNC):c.3499C>T (p.Arg1167Cys)	rs766439553	0.00002
NM_001458.5(FLNC):c.1571A>G (p.Lys524Arg)	rs753176255
NM_001458.5(FLNC):c.4566G>T (p.Gln1522His)	rs559667295
NM_001458.5(FLNC):c.4708G>T (p.Gly1570Cys)	rs1562999563
NM_001458.5(FLNC):c.6947A>G (p.Lys2316Arg)	rs1563003855
NM_001458.5(FLNC):c.7427A>G (p.His2476Arg)	rs1563005164

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