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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL4B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+4 more
GBenign/Likely benign
CUL4B
(L453F +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL4B
Duplication
(intron variant)
not specified
+2 more
GBenign/Likely benign
CUL4B
(Q218K +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL4B
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
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