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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
G6PC3
Single nucleotide variant
(5 prime UTR variant +1 more)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
GUncertain significance
G6PC3
(F309C +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
+2 more
GConflicting classifications of pathogenicity