| | PCDHG@, PCDHGA1 +17 more (V452G) | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder | |
| | PCDHG@, PCDHGA1 +21 more (R222H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (T184I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P174S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (N165H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (P160L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R141P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (R118C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (V106A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (H573D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +20 more (G306W) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +20 more (S231F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +20 more (P581T) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +20 more (L443F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +20 more (R439S) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +20 more (V425F) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +19 more (I320F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (S247Y) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (R187Q) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (N89S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (G9R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (E82K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (A806T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (S784R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (L695I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (T691A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (P683R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (S585P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (Q566R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (I319T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (L302V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (V211I) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (N905S +14 more) | Single nucleotide variant (missense variant) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (D799G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (N762D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (A712V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (L66R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (D634V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (V61A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +16 more (S488F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (A329T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (G305R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (N274S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (D219E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (A206S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (A157P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (M110T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (G650S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (P568S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (P466S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (T423S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (G306R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (A29T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (P175T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (S82R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (N79K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (L792P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (H756P) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (H756D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (A700T) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (V593F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (R581C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (L405V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (D205N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (Y174H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (V150A) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (I805V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (L78V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (V712L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (C706F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (E629D) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (F621C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (V550L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (Y493C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (P435R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (S818R +14 more) | Single nucleotide variant (missense variant) | not specified | |
| | PCDHG@, PCDHGA1 +15 more (E275K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +20 more (R623Q) | Single nucleotide variant (missense variant +1 more) | PCDHGC4-related disorder | |
| | PCDHG@, PCDHGA1 +20 more (S652I) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | PCDHG@, PCDHGA1 +20 more (V698L) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | PCDHG@, PCDHGA1 +21 more (E401V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (Q243H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (L609F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (E672K) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (S136R) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +20 more (A478E) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +16 more (V364E) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (L792F) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +17 more (P362L) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +19 more (K307N) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +18 more (V64G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | PCDHG@, PCDHGA1 +21 more (Q800K +14 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PCDHG@, PCDHGA1 +19 more (P524H) | Single nucleotide variant (missense variant +1 more) | not specified | |