RS139767162 KCNV2

Health Risk Chr 9:2719094
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Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in KCNV2
rs104894114 rs104894115 rs104894116 rs1402837406 rs104894113 rs149648640 rs387907302 rs786205121 rs140256288 rs145731729
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