RS398124234 FTCD
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Glutamate formiminotransferase deficiency
Inborn genetic diseases
FTCD-related disorder
Glutamate formiminotransferase deficiency
Inborn genetic diseases
FTCD-related disorder
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Formiminoglutamate levels | GC | OR: 1.03 | 4E-13 | PubMed |
Other Variants in FTCD