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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIN3
Single nucleotide variant
(synonymous variant)
not provided
GBenign
SYNE3, TC2N
+66 more
Duplication
not provided
GUncertain significance
ASB2, ATXN3
+42 more
Duplication
Achondrogenesis, type IA
GUncertain significance
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