List of variants reported as uncertain significance for Familial isolated congenital asplenia

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002295.6(RPSA):c.498+8T>A	rs754699583	0.00003
NM_004387.4(NKX2-5):c.707C>A (p.Pro236His)	rs397515399	0.00001
NM_002295.6(RPSA):c.491A>T (p.Asn164Ile)
NM_002295.6(RPSA):c.508T>G (p.Ser170Ala)

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