"GeneDx"[submitter] AND "LOC130005368"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1201613	NM_012250.6(RRAS2):c.62_73dup (p.Gly21_Gly24dup)	LOC130005368, RRAS2	Duplication (inframe_insertion +1 more)	not provided	GLikely pathogenic
Select item 2446526	NM_012250.6(RRAS2):c.71G>A (p.Gly24Asp)	LOC130005368, RRAS2 (G24D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 1699117	NM_012250.6(RRAS2):c.68G>A (p.Gly23Asp)	LOC130005368, RRAS2 (G23D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 626911	NM_012250.6(RRAS2):c.68G>T (p.Gly23Val)	LOC130005368, RRAS2 (G23V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 1342092	NM_012250.6(RRAS2):c.67G>T (p.Gly23Cys)	LOC130005368, RRAS2 (G23C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 1252817	NM_001177314.2(RRAS2):c.3+5109C>T	LOC130005368, RRAS2	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar