ClinVar Miner

List of variants in gene combination BRAF, LOC126860202 reported as uncertain significance for Noonan syndrome

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.995C>T (p.Thr332Ile)	rs1008080053	0.00004
NM_004333.6(BRAF):c.1056T>A (p.Asp352Glu)	rs1398817791

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