Related gene-specific medical variations for Gene (Select 25911) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2460418	NM_015448.3(DPCD):c.63C>A (p.Asp21Glu)	DPCD, LOC130004559 (D21E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234084	NM_015448.3(DPCD):c.53T>C (p.Leu18Pro)	DPCD, LOC130004559 (L18P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 91991	NM_015448.3(DPCD):c.11C>T (p.Thr4Met)	LOC130004559, DPCD (T4M)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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