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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QBP, LOC130060075
(R6L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
C1QBP, LOC130060075
Single nucleotide variant
(5 prime UTR variant)
C1QBP-related disorder
GLikely benign