ClinVar Miner

List of variants reported as pathogenic for LEOPARD syndrome 2

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1837C>G (p.Leu613Val)	rs80338797
NM_002880.4(RAF1):c.770C>T (p.Ser257Leu)	rs80338796
NM_002880.4(RAF1):c.776C>A (p.Ser259Tyr)	rs397516827

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