Related gene-specific medical variations for Gene (Select 6016) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247868	NC_000001.10:g.(?_155870179)_(155874615_?)dup	RIT1	Duplication	Noonan syndrome 8	GUncertain significance
Select item 3065119	NM_006912.6(RIT1):c.520G>A (p.Val174Ile)	RIT1 (V138I +2 more)	Single nucleotide variant (missense variant)	Noonan syndrome 8	GUncertain significance
Select item 2689872	NM_006912.6(RIT1):c.365G>A (p.Arg122Gln)	RIT1 (R122Q +2 more)	Single nucleotide variant (missense variant)	Noonan syndrome 8	GUncertain significance

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