ROGDI Chromosome 16

Rogdi atypical leucine zipper
52 variants 52 Health Risk

Upload your DNA to see your personal genotypes for variants in ROGDI.

What This Gene Does
Involved in brain development; neurogenesis; and odontogenesis of dentin-containing tooth. Located in nuclear envelope. Implicated in Kohlschutter-Tonz syndrome. [provided by Alliance of Genome Resources, Jul 2025]
Associated Conditions (4)
Amelocerebrohypohidrotic syndrome
ROGDI-related disorder
Inborn genetic diseases
Gastric cancer
Key Variants
RS142481526
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, ROGDI-related disorder, Amelocerebrohypohidrotic syndrome
Health Risk
RS143000899
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS144581570
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS144866271
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, ROGDI-related disorder, Amelocerebrohypohidrotic syndrome
Health Risk
RS145588848
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS148051351
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, ROGDI-related disorder, Amelocerebrohypohidrotic syndrome
Health Risk
RS200558978
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS201213891
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS2082694697
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Inborn genetic diseases, Amelocerebrohypohidrotic syndrome
Health Risk
RS371432203
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
RS371783831
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Inborn genetic diseases, Amelocerebrohypohidrotic syndrome
Health Risk
RS372520122
Conflicting classifications of pathogenicity
Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
Health Risk
All Variants (52)
RSID Category Clinical Significance Conditions
RS372097881 Health Risk Pathogenic/Likely pathogenic Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
RS786205124 Health Risk Pathogenic/Likely pathogenic Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome, Amelocerebrohypohidrotic syndrome
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