Related gene-specific medical variations for Gene (Select 84933) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3136095	NM_032847.3(C8orf76):c.556G>C (p.Ala186Pro)	C8orf76, ZHX1-C8orf76 (A154P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369584	NM_032847.3(C8orf76):c.22T>G (p.Phe8Val)	C8orf76, ZHX1-C8orf76 (F8V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance