| | LHCGR, STON1-GTF2A1L (A689T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (F667L) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (L607V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (N507S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (G489V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (T469I) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (A442T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (T441I) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (Q421H) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (S420F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (M408I) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LHCGR, STON1-GTF2A1L (R395C) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (V380A) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (R342Q) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (I249T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (L242V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (T197M) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (E148V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (L97F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (I78V) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (S66P) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LHCGR, STON1-GTF2A1L (R23G) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |