| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | KLF1, LOC117125591 (R340H) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | KLF1, LOC117125591 (T302K) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | KLF1, LOC117125591 (T251I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | KLF1, LOC117125591 (T243M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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