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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DLL3, LOC130064417
(L142Q)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
DLL3, LOC130064417
+1 more
(F172C)
Single nucleotide variant
(missense variant)
not specified
+4 more
GBenign
DLL3, LOC130064417
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign
DLL3, LOC130064417
(P206A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
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