| | ZNF337-AS1, ZNF337 (R740H) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R740G) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (R740C) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R720L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (W676R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (Q663R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (V660A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (S651L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (P571L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (R570K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (Q548P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (H510Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R495Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (V448M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (I442N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (S412R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (G389V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (A377V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (E373K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R355Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (H338Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (T330A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (E324Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (P319T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (P319A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (N308D) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R299Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (G288R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337-AS1, ZNF337 (Y273C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (Q215R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (F208V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (H198Y) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R191Q) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (R185H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (V168L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (T163R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ZNF337, ZNF337-AS1 (V149I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |