List of variants in gene RAF1 reported as uncertain significance for LEOPARD syndrome 2; Noonan syndrome 5

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe)	rs730881004	0.00006
NM_002880.4(RAF1):c.1922C>G (p.Thr641Arg)	rs587777587
NM_002880.4(RAF1):c.1A>G (p.Met1Val)	rs2125453796

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