GAD2
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs10421…
GCLC
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Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs12524…
GCLM
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Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs23010…
GDF5
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs14338…
GGH
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs18009…
GPX1
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs10504…
GPX3
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs38298…
GPX4
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs20744…
GSR
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs10021…
GSTM1
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs10568…
GSTO1
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs11509…
GSTP1
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Questions for your visit
Is this a common marker, a pathogenic variant, or an uncertain finding? Does it change my care? Would confirmation or genetic counseling be useful?
rs11382…
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