RS199889415 MED13

Health Risk Chr 17:61982338
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Associated Conditions
Inborn genetic diseases
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Inborn genetic diseases
See cases
Other Variants in MED13
rs773685207 rs1567938478 rs1567940265 rs1044065786 rs1567975588 rs780070113 rs1603405457 rs2080047817 rs1603392097 rs1603392856
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