RS606231473 CSF3R
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Other Variants in CSF3R