| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | IL16, LOC126862197
+1 more (F175S) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | IL16, LOC126862197
+1 more (R199Q) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided | |
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