ClinVar Miner

List of variants in gene RAF1 reported as uncertain significance by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.29C>T (p.Thr10Met)	rs144637992	0.00001
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn)	rs773583951

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