- The following term was not found in ClinVar: rs10039029.
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | Mitochondrial complex II deficiency, nuclear type 1 +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Hereditary cancer-predisposing syndrome +6 more | |
Click to view in NCBI Gene