List of variants reported as likely pathogenic for LEOPARD syndrome 1 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002834.5(PTPN11):c.1471C>A (p.Pro491Thr)	rs397507539
NM_002834.5(PTPN11):c.1472C>A (p.Pro491His)	rs397507540
NM_002834.5(PTPN11):c.691C>T (p.Arg231Ter)	rs2038154558
NM_002834.5(PTPN11):c.802G>A (p.Gly268Ser)	rs397507527

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