Related gene-specific medical variations for Gene (Select 160851) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3081918	NM_178009.5(DGKH):c.138G>C (p.Glu46Asp)	DGKH, LOC130009645 (E46D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610138	NM_178009.5(DGKH):c.24C>G (p.His8Gln)	DGKH, LOC130009645 (H8Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283907	NM_178009.5(DGKH):c.59G>C (p.Gly20Ala)	DGKH, LOC130009645 (G20A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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