RS878855224 DIS3L2

Health Risk Chr 2:232334479
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Perlman syndrome
Perlman syndrome
Other Variants in DIS3L2
rs1489037110 rs201733073 rs202042951 rs201719374 rs186865544 rs754433044 rs775814377 rs186340144 rs368518323 rs2697798
Ask Dr. Hemsworth about this variant