Related gene-specific medical variations for Gene (Select 81552) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2533246	NM_030796.5(VOPP1):c.22G>A (p.Val8Met)	LOC129998485, VOPP1 (V8M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2324337	NM_030796.5(VOPP1):c.40G>C (p.Gly14Arg)	LOC129998485, VOPP1 (G14R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance