| | UGT2B11, LOC105377267 (W463S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (R459Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (L429P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (N418H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (P400S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (H386Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (W356C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (N350S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (L349I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (I324V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (H281Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (V277I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (F276L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (V274I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (F264I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (P243S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (D228E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (L218I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (Y216H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (P191S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (I180V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (A162V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (R144I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (Q141L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (Y120H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (L119F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (F109I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (I89V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (N88S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (E87G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (F74L) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | UGT2B11, LOC105377267 (K73N) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (S61T) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (E32V) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (G21A) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | LOC105377267, UGT2B11 (V8A) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |