RS786203999 GPT2

Health Risk Chr 16:46906858
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What This Variant Does
"CLNSIG=5
Associated Conditions
Glutamate pyruvate transaminase 2 deficiency
Inborn genetic diseases
Glutamate pyruvate transaminase 2 deficiency
Inborn genetic diseases
Other Variants in GPT2
rs2548985626 rs2548963176 rs2548989725 rs2548982827 rs1596864597 rs2548953788 rs745565332 rs778445616 rs190315044 rs781387019
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