RS761368190 ACO2

Health Risk Chr 22:41522872
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in ACO2
rs786200924 rs387907389 rs141772938 rs752034900 rs786204828 rs786204829 rs786204830 rs747330606 rs863223881 rs864309499
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