ClinVar for MedGen (Select 277970) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 15904	NM_002070.4(GNAI2):c.536G>A (p.Arg179His)	GNAI2 (R179H +4 more)	Single nucleotide variant (missense variant)	Ovarian granulosa cell tumor +2 more	GPathogenic
Select item 15903	NM_002070.4(GNAI2):c.535C>T (p.Arg179Cys)	GNAI2 (R179C +4 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity