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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CSF3R
(E808K +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary neutrophilia
+3 more
GBenign/Likely benign
CSF3R
(W547*)
Single nucleotide variant
(nonsense)
not provided
+4 more
GPathogenic/Likely pathogenic
CSF3R
Single nucleotide variant
(splice donor variant)
Hereditary neutrophilia
+1 more
GPathogenic/Likely pathogenic
CSF3R
(A119T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
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