RS202080221 SH2B3
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What This Variant Does
"CLNSIG=255
Associated Conditions
Thrombocythemia 1
Hepatoblastoma
Primary myelofibrosis
Hereditary cancer
Primary familial polycythemia due to EPO receptor mutation
Thrombocythemia 1
Hepatoblastoma
Primary myelofibrosis
Hereditary cancer
Primary familial polycythemia due to EPO receptor mutation
Other Variants in SH2B3