Variants in gene BRAF with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1433-19A>G	rs369635503	0.00112
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn)	rs397507456	0.00030
NM_004333.6(BRAF):c.138+17C>G	rs756400234	0.00003
NM_004333.6(BRAF):c.968C>T (p.Ser323Leu)	rs397516907	0.00001
NM_004333.6(BRAF):c.68T>A (p.Met23Lys)	rs746778122
NM_004333.6(BRAF):c.83GCGCCG[2] (p.28GA[2])	rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4])	rs397507458

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