List of variants in gene BRAF reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

Minimum submission review status:		Collection method:
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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1929A>G (p.Gly643=)	rs9648696	0.30796
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp)	rs371877084	0.01088
NM_004333.6(BRAF):c.1383A>G (p.Gln461=)	rs56216404	0.00399
NM_004333.6(BRAF):c.1227A>G (p.Ser409=)	rs145035762	0.00318
NM_004333.6(BRAF):c.1332G>A (p.Arg444=)	rs56101602	0.00068
NM_004333.6(BRAF):c.2235A>G (p.Leu745=)	rs56046546	0.00030
NM_004333.6(BRAF):c.1992+16G>C	rs3789806

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