RS606231475 CSF3R

Health Risk Chr 1:36472272
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Other Variants in CSF3R
rs121918426 rs606231474 rs606231473 rs796065343 rs879253750 rs148104401 rs368290894 rs139332126 rs148307285 rs141619366
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