ClinVar for MedGen (Select 1684730) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2576594	NM_012250.6(RRAS2):c.560C>G (p.Pro187Arg)	RRAS2 (P110R +2 more)	Single nucleotide variant (missense variant)	Noonan syndrome 12	GUncertain significance
Select item 2445986	NM_012250.6(RRAS2):c.439C>T (p.Arg147Trp)	RRAS2 (R147W +2 more)	Single nucleotide variant (missense variant)	RRAS2-related disorder +1 more	GUncertain significance
Select item 2444166	NM_012250.6(RRAS2):c.67G>A (p.Gly23Ser)	LOC130005368, RRAS2 (G23S)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome 12 +1 more	GConflicting classifications of pathogenicity
Select item 1699117	NM_012250.6(RRAS2):c.68G>A (p.Gly23Asp)	LOC130005368, RRAS2 (G23D)	Single nucleotide variant (missense variant +1 more)	Noonan syndrome 12 +1 more	GPathogenic
Select item 1270813	NM_012250.6(RRAS2):c.409-16A>T	RRAS2	Single nucleotide variant (intron variant)	Noonan syndrome 12 +1 more	GBenign
Select item 626913	NM_012250.6(RRAS2):c.70_78dup (p.Gly24_Gly26dup)	LOC130005368, RRAS2	Duplication (inframe_insertion +1 more)	Noonan syndrome +3 more	GPathogenic
Select item 626912	NM_012250.6(RRAS2):c.208G>A (p.Ala70Thr)	RRAS2 (A35T +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	Noonan syndrome +1 more	GConflicting classifications of pathogenicity
Select item 9447	NM_012250.6(RRAS2):c.215A>T (p.Gln72Leu)	RRAS2 (Q37L +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	Noonan syndrome +1 more	GPathogenic

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