List of variants in gene BRAF reported as benign by PreventionGenetics, part of Exact Sciences

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: 17

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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.1518-48C>T	rs62487918	0.05391
NM_004333.6(BRAF):c.980+27G>A	rs41282721	0.05356
NM_004333.6(BRAF):c.1517+35G>C	rs71645981	0.01493
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.712-40T>A	rs71645952	0.00952
NM_004333.6(BRAF):c.1315-18T>G	rs6959000	0.00840
NM_004333.6(BRAF):c.1141-19C>T	rs71645959	0.00360
NM_004333.6(BRAF):c.1227A>G (p.Ser409=)	rs145035762	0.00318
NM_004333.6(BRAF):c.1517+20T>C	rs71645980	0.00273
NM_004333.6(BRAF):c.2127+3A>G	rs371976102	0.00043
NM_004333.6(BRAF):c.2235A>G (p.Leu745=)	rs56046546	0.00030
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn)	rs397507456	0.00025
NM_004333.6(BRAF):c.-5A>G	rs71645936	0.00024
NM_004333.6(BRAF):c.968C>T (p.Ser323Leu)	rs397516907	0.00012
NM_004333.6(BRAF):c.1992+16G>C	rs3789806

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