Related gene-specific medical variations for Gene (Select 100134713) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3187851	NM_004546.3(NDUFB2):c.62G>A (p.Gly21Asp)	LOC129999506, NDUFB2 +1 more (G21D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3187850	NM_004546.3(NDUFB2):c.61G>C (p.Gly21Arg)	LOC129999506, NDUFB2 +1 more (G21R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2488356	NM_004546.3(NDUFB2):c.84T>G (p.Asp28Glu)	LOC129999506, NDUFB2 +1 more (D28E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208003	NM_004546.3(NDUFB2):c.70C>T (p.Arg24Trp)	LOC129999506, NDUFB2 +1 more (R24W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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