RS118203971 G6PC3

Health Risk Chr 17:44075786
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
Other Variants in G6PC3
rs118203968 rs118203969 rs118203970 rs267606834 rs200478425 rs775224457 rs769441127 rs148559256 rs797044567 rs140294222
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