| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EGFLAM, EGFLAM-AS1
+1 more (L392P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | EGFLAM, EGFLAM-AS1
+1 more (F441S +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC126807366, EGFLAM
+1 more (L432F +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | EGFLAM, EGFLAM-AS1
+1 more (E672D +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene