List of variants reported as likely benign for Dilated cardiomyopathy 1L; Autosomal recessive limb-girdle muscular dystrophy type 2F by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000337.6(SGCD):c.507G>A (p.Ala169=)	rs10071079	0.00680
NM_000337.6(SGCD):c.699+71G>A	rs187204080	0.00245
NM_000337.5(SGCD):c.-404G>A	rs192662989	0.00016
NM_000337.6(SGCD):c.3+11C>T	rs374790317	0.00010
NM_000337.6(SGCD):c.393C>T (p.Ala131=)	rs397517922	0.00004

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