List of variants reported as uncertain significance for B cell deficiency by Paediatric Laboratory, Institute for Maternal and Child Health - IRCCS Burlo Garofolo

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003998.4(NFKB1):c.2504C>T (p.Thr835Ile)
NM_005026.5(PIK3CD):c.1116G>C (p.Lys372Asn)

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