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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC107548112, REN
Single nucleotide variant
(synonymous variant)
REN-related disorder
+2 more
GConflicting classifications of pathogenicity
LOC107548112, REN
(P8A)
Single nucleotide variant
(missense variant)
not specified
+5 more
GBenign/Likely benign