R42Q (p.Arg42Gln) variant of FLG (Filaggrin)
R42Q (p.Arg42Gln) in FLG (Filaggrin) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes population frequency data.
R42Q (p.Arg42Gln) variant details
- p.Arg42Gln
- ExAC rs771075649
- TOPMed rs771075649
- gnomAD rs771075649
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Population evidence available