Related gene-specific medical variations for Gene (Select 56674) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2311930	NM_020644.3(TMEM9B):c.96C>A (p.Asp32Glu)	LOC130005257, TMEM9B (D32E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2219277	NM_020644.3(TMEM9B):c.95A>T (p.Asp32Val)	LOC130005257, TMEM9B (D32V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance