| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | AMH, LOC130063038
+1 more (D192G) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +1 more | |
| | AMH, LOC130063038
+1 more (P203S) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene