Related gene-specific medical variations for Gene (Select 53826) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3097577	NM_022003.4(FXYD6):c.257A>G (p.Asn86Ser)	FXYD6, FXYD6-FXYD2 (M74V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464690	NM_022003.4(FXYD6):c.253G>A (p.Ala85Thr)	FXYD6, FXYD6-FXYD2 (A85T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance