Related gene-specific medical variations for Gene (Select 339453) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2437114	NM_001114748.2(TMEM240):c.217G>A (p.Ala73Thr)	TMEM240 (A73T)	Single nucleotide variant (missense variant)	Spinocerebellar ataxia type 21	GUncertain significance
Select item 1295591	NM_001114748.2(TMEM240):c.164+193C>G	LOC121967044, TMEM240	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 806035	NM_001114748.2(TMEM240):c.408C>A (p.Ser136Arg)	TMEM240 (S136R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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