Related gene-specific medical variations for Gene (Select 93624) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2529529	NM_152293.3(TADA2B):c.200A>C (p.Glu67Ala)	LOC100129931, TADA2B (E67A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264338	NM_152293.3(TADA2B):c.191C>G (p.Pro64Arg)	LOC100129931, TADA2B (P64R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance