| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +2 more | |
| | | Single nucleotide variant (synonymous variant) | GRN-related frontotemporal lobar degeneration with Tdp43 inclusions +4 more | |
| | | Microsatellite (splice donor variant) | Inborn genetic diseases +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene