| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GLA, RPL36A-HNRNPH2 (G366D) | Single nucleotide variant (missense variant +2 more) | Fabry disease +1 more | GPathogenic/Likely pathogenic |
| | RPL36A-HNRNPH2, GLA (P293L +1 more) | Single nucleotide variant (missense variant +2 more) | Fabry disease | |
Click to view in NCBI Gene