RS201279487 DIS3L2

Health Risk Chr 2:232087572
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Associated Conditions
Perlman syndrome
Inborn genetic diseases
Perlman syndrome
Inborn genetic diseases
Other Variants in DIS3L2
rs1489037110 rs201733073 rs202042951 rs201719374 rs186865544 rs754433044 rs775814377 rs186340144 rs368518323 rs878855224
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