List of variants in gene RRAS2 reported as uncertain significance for Noonan syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012250.6(RRAS2):c.440G>A (p.Arg147Gln)	rs377321245	0.00006
NM_012250.6(RRAS2):c.139A>G (p.Ile47Val)
NM_012250.6(RRAS2):c.560C>G (p.Pro187Arg)	rs2494095831

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