| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130065272, SRXN1 (A14G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130065272, SRXN1 (E20G) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | LOC130065272, SRXN1 (G31C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130065272, SRXN1 (A14E) | Single nucleotide variant (missense variant) | not specified | |
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