RS1776309065 CYP21A2

Health Risk Chr 6:32041003
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CYP21A2
rs6475 rs6471 rs9378251 rs6467 rs201552310 rs397509367 rs6445 rs387906510 rs1474566961 rs7755898
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