| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129935417, TMEM237 (E11Q) | Single nucleotide variant (missense variant) | TMEM237-related disorder | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +1 more | |
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