RS587777238 FAM111B

Health Risk Chr 11:59125980
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
Other Variants in FAM111B
rs587777236 rs587777237 rs1555014282 rs1565191262 rs2135404946 rs2135405575
Ask Dr. Hemsworth about this variant