Related gene-specific medical variations for Gene (Select 85359) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271694	NM_033257.4(DGCR6L):c.113C>T (p.Ser38Phe)	DGCR6L, LOC130066993 (S38F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081852	NM_033257.4(DGCR6L):c.155C>A (p.Ala52Asp)	DGCR6L, LOC130066993 (A52D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548523	NM_033257.4(DGCR6L):c.27G>T (p.Glu9Asp)	DGCR6L, LOC130066993 (E9D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532724	NM_033257.4(DGCR6L):c.163C>T (p.Leu55Phe)	DGCR6L, LOC130066993 (L55F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710255	NM_033257.4(DGCR6L):c.216C>T (p.His72=)	DGCR6L, LOC125424388	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 161788	NM_033257.4(DGCR6L):c.608C>T (p.Pro203Leu)	DGCR6L (P203L)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar