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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CEBPZ, LOC126806192
+1 more
(E19D)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
CEBPZ, LOC126806192
+1 more
(P15S)
Single nucleotide variant
(missense variant)
not provided
GBenign
CEBPZ, LOC126806192
+1 more
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign
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