RS398124234 FTCD

Health Risk Chr 21:46145925
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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
rs140217223 rs2079131229 rs777286639 rs2517047371 rs1355632505 rs776381858 rs1310075515 rs369754449 rs377359525 rs777099958
Ask Dr. Hemsworth about this variant