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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004755, SHOC2
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
+1 more
GConflicting classifications of pathogenicity
LOC130004755, SHOC2
Single nucleotide variant
(intron variant)
not provided
GBenign