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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS45
(I82M +1 more)
Single nucleotide variant
(missense variant +1 more)
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
+1 more
GBenign
VPS45
Single nucleotide variant
(intron variant)
Congenital neutropenia-myelofibrosis-nephromegaly syndrome
+1 more
GBenign/Likely benign