RS368215361 ATP2B3

Health Risk Chr X:153565099
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in ATP2B3
rs397514619 rs724160009 rs724160011 rs724160012 rs782596945 rs781901998 rs149114271 rs1603040061 rs782756404 rs2124491843
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