ClinVar Miner

List of variants in gene combination BRAF, LOC126860202 reported as benign for RASopathy

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.981-20C>T	rs374896031	0.00066
NM_004333.6(BRAF):c.1068A>G (p.Gln356=)	rs143335467	0.00003

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