ClinVar Miner

List of variants reported as uncertain significance for Familial hemophagocytic lymphohistiocytosis 2 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001083116.3(PRF1):c.542T>C (p.Phe181Ser)	rs770131011	0.00002
NM_001083116.3(PRF1):c.47C>T (p.Pro16Leu)	rs751379475
NM_001083116.3(PRF1):c.647T>C (p.Ile216Thr)

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