List of variants in gene BRAF reported as benign for Noonan syndrome with multiple lentigines

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1929A>G (p.Gly643=)	rs9648696	0.30275
NM_004333.6(BRAF):c.-19C>T	rs71645935	0.01115
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_004333.6(BRAF):c.*387G>A	rs114105685	0.00981
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00771
NM_004333.6(BRAF):c.1383A>G (p.Gln461=)	rs56216404	0.00373
NM_004333.6(BRAF):c.1332G>A (p.Arg444=)	rs56101602	0.00068
NM_004333.6(BRAF):c.2127+3A>G	rs371976102	0.00043
NM_004333.6(BRAF):c.2235A>G (p.Leu745=)	rs56046546	0.00040
NM_004333.6(BRAF):c.-5A>G	rs71645936	0.00024
NM_004333.6(BRAF):c.1694+14G>A	rs184144181	0.00010
NM_004333.6(BRAF):c.708C>T (p.Asn236=)	rs138333692	0.00010
NM_004333.6(BRAF):c.*111C>T	rs539860876

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