| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126862416, HSD17B2 (M189T) | Single nucleotide variant (missense variant) | not specified | |
| | HSD17B2, LOC126862416 (S218R) | Single nucleotide variant (missense variant) | not specified | |
| | HSD17B2, LOC126862416 (V199A) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not provided | |
| | HSD17B2, LOC126862416 (L204F) | Single nucleotide variant (missense variant) | not specified | |
| | HSD17B2, LOC126862416 (T175S) | Single nucleotide variant (missense variant) | not specified | |
| | HSD17B2, LOC126862416 (L179F) | Single nucleotide variant (missense variant) | not specified | |
| | HSD17B2, LOC126862416 (P174L) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
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