List of variants in gene BRAF reported as likely benign for Noonan syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_004333.6(BRAF):c.101C>T (p.Ala34Val)	rs1424449802	0.00001
NM_004333.6(BRAF):c.2128-5del	rs373442098
NM_004333.6(BRAF):c.83GCGCCG[1] (p.28GA[1])	rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4])	rs397507458

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