RS80338899 FAH

Health Risk Chr 15:80173093
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What This Variant Does
"Identification of a stop mutation in five Finnish patients suffering from hereditary tyrosinemia typ...
Associated Conditions
Tyrosinemia type I
Tyrosinemia type I
Other Variants in FAH
rs121965073 rs121965074 rs121965076 rs80338900 rs80338901 rs121965075 rs121965077 rs80338895 rs121965078 rs80338894
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