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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLN5, LOC130009913
Single nucleotide variant
(synonymous variant)
not specified
+4 more
GBenign/Likely benign
CLN5, LOC130009913
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign