| | ADGRL1, ADGRL1-AS1 (Q1464P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1448E +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P1441S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (Y1435C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (Y1423F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E1421D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1410T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S1401G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P1400A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S1400N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (D1394N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P1398R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P1395S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (Y1380C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (L1379V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1381G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1368Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G1364S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E1367Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (C1364Y +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (D1352N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1330Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G1322V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1-AS1, ADGRL1 (G1321R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G1317R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V1313M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V1284M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1272Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1272W +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S1251T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P1238T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | ADGRL1, ADGRL1-AS1 (E1201K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1189C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1162T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T1161M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G1139fs +1 more) | Deletion (frameshift variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T1127A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R1115P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S1110C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1050T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1050V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (F1013V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (I980V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G969S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R962C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S939C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (L904F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (N888S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S856* +1 more) | Single nucleotide variant (nonsense) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E852G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R843H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R843C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S817L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V774I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A759T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G749S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A743D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P703L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E694K +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E682Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E631D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V615M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R596H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S566F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A567T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R557Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (H555R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R559Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (I553V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A541S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R503Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (L493V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R487Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R466Q +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P452S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R435H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A424T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S427L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T423P +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S403A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S397G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R386H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R386C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (N386S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V367I +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders +1 more | |
| | ADGRL1, ADGRL1-AS1 (R349C +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R343H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A334V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V328M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V316M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S316F +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (D306N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T278S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R256H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S253L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T247M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (G245R +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R231H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |