List of variants reported as uncertain significance for Dilated cardiomyopathy 1X; Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4; Autosomal recessive limb-girdle muscular dystrophy type 2M; Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4 by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.1159G>A (p.Gly387Arg)	rs148975262	0.00048
NM_001079802.2(FKTN):c.397A>G (p.Met133Val)	rs569778463	0.00004
NM_001079802.2(FKTN):c.1186A>C (p.Lys396Gln)	rs1477740717	0.00001
NM_001079802.2(FKTN):c.802G>T (p.Val268Leu)	rs878854165	0.00001
NM_001079802.2(FKTN):c.374G>T (p.Gly125Val)	rs142783718
NM_001079802.2(FKTN):c.911-13A>G	rs766103012

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