| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Duplication | not provided | |
| | LOC129933002, RNASEH1 (A14T) | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | LOC129933002, RNASEH1 (S22C) | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases | |
| | LOC129933002, RNASEH1 (H9Y) | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases | |
| | LOC129933002, RNASEH1 (S22F) | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | |
| | LOC129933002, RNASEH1 (R23H) | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases +1 more | |
| | LOC129933002, RNASEH1 (S2T) | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | LOC129933002, RNASEH1 (R20C) | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
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