List of variants reported as uncertain significance for hemophagocytic syndrome by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_003764.4(STX11):c.616G>A (p.Glu206Lys)	rs145347140	0.00086
NM_001083116.3(PRF1):c.1262T>G (p.Phe421Cys)	rs200534908	0.00014
NM_000081.4(LYST):c.949G>A (p.Glu317Lys)	rs201337542	0.00008
NM_001083116.3(PRF1):c.1097A>G (p.Gln366Arg)	rs957245579	0.00001

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