RS121918426 CSF3R

Health Risk Chr 1:36467597
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary neutrophilia
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
CSF3R-related disorder
Hereditary neutrophilia
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
CSF3R-related disorder
Other Variants in CSF3R
rs606231474 rs606231475 rs606231473 rs796065343 rs879253750 rs148104401 rs368290894 rs139332126 rs148307285 rs141619366
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