| | | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (R1108H +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (H1109Y +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (Y131*) | Single nucleotide variant (non-coding transcript variant +1 more) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (V328M +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R231H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (V206fs +1 more) | Insertion (frameshift variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A194V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (L139P +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 (Y1380C +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 (V1284M +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 (I980V +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 (S856* +1 more) | Single nucleotide variant (nonsense) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A759T +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 (S566F +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 | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (S403A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (T637R +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADGRL1, ADGRL1-AS1 (S1218G +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | ADGRL1-AS1, ADGRL1 (G882W +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (L1379R +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (V757fs +1 more) | Deletion (frameshift variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (P208R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (S1001R +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (D1377E +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (I237T +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (P1238T +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | ADGRL1, ADGRL1-AS1 (Q125fs) | Duplication (non-coding transcript variant +1 more) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (R224H +1 more) | Single nucleotide variant (missense variant) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | ADGRL1, ADGRL1-AS1 (V1086fs +1 more) | Duplication (non-coding transcript variant +1 more) | Developmental delay, behavioral abnormalities, and neuropsychiatric disorders | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (V1284A +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (R1143* +1 more) | Single nucleotide variant (nonsense) | Neurodevelopmental disorder | |
| | ADGRL1, ADGRL1-AS1 (V134L +1 more) | Single nucleotide variant (missense variant) | not provided | |
| | ADGRL1, ADGRL1-AS1 (S817L +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 (L143R +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 (G749S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R478* +1 more) | Single nucleotide variant (nonsense) | not provided | |
| | ADGRL1, ADGRL1-AS1 (A743D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (A1050V +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 (R435H +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R210H +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 (F1013V +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 (V218I +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 (A1050T +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 (G245R +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 (S1400N +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 (Y1423F +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 (T247M +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, ADGRL1-AS1 (A1410T +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 (R183C +1 more) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | ADGRL1, ADGRL1-AS1 (A334V +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 (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 (R1381G +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (P452S +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (R466Q +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 (D1352N +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 (T1127A +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 (E1421D +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 (Q1464P +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 (I553V +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 (V367I +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (E1201K +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 (E631D +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | ADGRL1, ADGRL1-AS1 (D306N +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |