RS587777237 FAM111B

Health Risk Chr 11:59125976
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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 rs587777238 rs1555014282 rs1565191262 rs2135404946 rs2135405575
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