RS2079442813 RNF213

Health Risk Chr 17:80369783
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in RNF213
rs112735431 rs397514563 rs139265462 rs797045187 rs148776624 rs201733659 rs189765261 rs1555675538 rs1555676035 rs1568149971
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