| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130063193, MAP2K2 (T17A) | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | LOC130063193, MAP2K2 (A11G) | Single nucleotide variant (missense variant) | not specified | |
| | | Microsatellite (5 prime UTR variant) | not specified | |
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