| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860809, WDR37 (T241A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860809, WDR37 (A229V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126860809, WDR37 (L232V) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126860809, WDR37 (D220G) | Single nucleotide variant (missense variant) | Neurooculocardiogenitourinary syndrome | |
| | | Single nucleotide variant (intron variant) | Neurooculocardiogenitourinary syndrome | |
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