| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130005945, RASGRP2 (C11S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC130005945, RASGRP2 (D6G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene