RS118203968 G6PC3

Health Risk Chr 17:44075759 snv missense variant
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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
Population Frequencies
gnomAD ALL
0%
Other Variants in G6PC3
rs118203969 rs118203970 rs118203971 rs267606834 rs200478425 rs775224457 rs769441127 rs148559256 rs797044567 rs140294222
Ask Dr. Hemsworth about this variant