| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | GUCY2C, GUCY2C-AS1 (S123T) | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (intron variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (intron variant) | Congenital diarrhea 6 +2 more | |
| | GUCY2C, GUCY2C-AS1 (F281L) | Single nucleotide variant (missense variant) | Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency +2 more | |
| | | Single nucleotide variant (intron variant) | Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency +2 more | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |
| | | Single nucleotide variant (missense variant) | Meconium ileus +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (intron variant) | Congenital diarrhea 6 +3 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Duplication (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Congenital diarrhea 6 | |