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Links from MedGen

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSEN15
(H116Y)
Single nucleotide variant
(missense variant +1 more)
Pontocerebellar hypoplasia, type 2F
GLikely pathogenic
TSEN15
(Y152C)
Single nucleotide variant
(missense variant +2 more)
Pontocerebellar hypoplasia, type 2F
GPathogenic
TSEN15
(W76G)
Single nucleotide variant
(missense variant +1 more)
Pontocerebellar hypoplasia, type 2F
GUncertain significance
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