Variants in gene BRAF with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001374258.1(BRAF):c.1529C>G (p.Thr510Arg)	rs397516891
NM_004333.6(BRAF):c.1742A>C (p.Asn581Thr)	rs121913370
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004333.6(BRAF):c.793G>C (p.Gly265Arg)	rs397516905
NM_004333.6(BRAF):c.826G>C (p.Val276Leu)	rs1057518105

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