Related gene-specific medical variations for Gene (Select 79627) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3302230	NM_024576.5(OGFRL1):c.204C>G (p.Asp68Glu)	LOC129996705, OGFRL1 (D68E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204151	NM_024576.5(OGFRL1):c.193C>G (p.Pro65Ala)	LOC129996705, OGFRL1 (P65A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204150	NM_024576.5(OGFRL1):c.143A>G (p.Glu48Gly)	LOC129996705, OGFRL1 (E48G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592069	NM_024576.5(OGFRL1):c.157C>A (p.Pro53Thr)	LOC129996705, OGFRL1 (P53T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283494	NM_024576.5(OGFRL1):c.80C>T (p.Ser27Leu)	LOC129996705, OGFRL1 (S27L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257864	NM_024576.5(OGFRL1):c.82G>A (p.Glu28Lys)	LOC129996705, OGFRL1 (E28K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar