CLOCK
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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?
rs18012…
COL5A1
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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?
rs12722…
COMT
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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?
rs16572…
CTH
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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?
rs10217…
CUBN
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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?
rs18012…
CYP19A1
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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?
rs10046…
CYP1A2
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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?
rs20695…
CYP1B1
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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…
CYP27B1
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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?
rs10877…
CYP2D6
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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?
rs10658…
DAOA
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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?
rs23911…
DHFR
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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?
rs16436…
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