List of variants reported as likely benign by ACT Genomics,

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001130009.3(GEN1):c.2619T>G (p.Ser873Arg)	rs57936182	0.00369
NM_024642.5(GALNT12):c.719C>T (p.Pro240Leu)	rs59362219	0.00016
NM_002485.5(NBN):c.1036G>A (p.Val346Met)	rs200297914	0.00011
NM_024675.4(PALB2):c.2474G>C (p.Arg825Thr)	rs146218439	0.00008
NM_000492.4(CFTR):c.2684G>A (p.Ser895Asn)	rs201864483

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