List of variants reported as uncertain significance for neuronal ceroid lipofuscinosis by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001371596.2(MFSD8):c.479C>T (p.Thr160Ile)	rs1162750836	0.00001
NM_002087.4(GRN):c.7A>G (p.Thr3Ala)	rs2048347394

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