| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130065313, TMEM239 (S113T +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130065313, TMEM239 (L104P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130065313, TMEM239 (T121M +1 more) | Single nucleotide variant (missense variant) | not specified | |
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