RS777099958 FTCD

Health Risk Chr 21:46138584
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What This Variant Does
"CLNSIG=5
Associated Conditions
Glutamate formiminotransferase deficiency
Inborn genetic diseases
Glutamate formiminotransferase deficiency
Inborn genetic diseases
Other Variants in FTCD
rs140217223 rs2079131229 rs777286639 rs2517047371 rs1355632505 rs776381858 rs1310075515 rs369754449 rs377359525 rs398124234
Ask Dr. Hemsworth about this variant