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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129936171, TSEN2
Single nucleotide variant
(5 prime UTR variant +1 more)
Pontoneocerebellar hypoplasia
+1 more
GBenign
LOC129936171, TSEN2
Deletion
(5 prime UTR variant +1 more)
not provided
GBenign