RS137853967 ATP13A2

Health Risk Chr 1:16986864
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What This Variant Does
"[OMIM:?]
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in ATP13A2
rs786205056 rs2100817106 rs121918227 rs762033589 rs587776890 rs587777053 rs144701072 rs142616130 rs55708915 rs568367953
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