RS1057521937 CYBB

Health Risk Chr X:37805085
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CYBB
rs137854585 rs137854586 rs137854588 rs137854589 rs137854590 rs137854591 rs137854596 rs2146821097 rs137854592 rs1602175016
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