G18D (p.Gly18Asp) variant of LRP4 (O75096)
G18D (p.Gly18Asp) in LRP4 (O75096) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes population frequency data and structural context.
G18D (p.Gly18Asp) variant details
- p.Gly18Asp
- 1000Genomes rs200914006
- TOPMed rs200914006
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Population evidence available
- Structural context available