Related gene-specific medical variations for Gene (Select 4715) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 802439	NC_000008.11:g.124567749C>T	MTSS1, NDUFB9	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 802438	NC_000008.11:g.124557903G>A	NDUFB9, MTSS1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 377380	NM_005005.3(NDUFB9):c.477G>C (p.Lys159Asn)	NDUFB9 (K159N +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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