ClinVar Miner

List of variants in gene RAF1 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002880.4(RAF1):c.1877A>G (p.His626Arg)	rs1553609795	0.00001
NM_002880.4(RAF1):c.1837C>A (p.Leu613Ile)	rs80338797
NM_002880.4(RAF1):c.781C>T (p.Pro261Ser)	rs121434594

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