Related gene-specific medical variations for Gene (Select 115752) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2613069	NM_001143688.3(DIS3L):c.5T>G (p.Leu2Arg)	DIS3L, LOC130057336 (L2R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2595091	NM_001143688.3(DIS3L):c.74A>G (p.His25Arg)	DIS3L, LOC130057336 (H25R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2489699	NM_001143688.3(DIS3L):c.16G>C (p.Glu6Gln)	DIS3L, LOC130057336 (E6Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2386812	NM_001143688.3(DIS3L):c.8A>C (p.Gln3Pro)	DIS3L, LOC130057336 (Q3P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2367133	NM_001143688.3(DIS3L):c.67C>T (p.Arg23Cys)	DIS3L, LOC130057336 (R23C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 980528	GRCh37/hg19 15q22.31(chr15:66563992-66625470)x1	DIS3L	Copy number loss	not provided	GUncertain significance
Select item 161529	NM_001143688.3(DIS3L):c.3089G>A (p.Gly1030Glu)	DIS3L (G1030E +6 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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