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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130006100, PACS1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
GLikely benign
LOC130006100, PACS1
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+1 more
GLikely benign