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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NR4A2
(C236F +1 more)
Single nucleotide variant
(missense variant)
Parkinson disease, late-onset
GPathogenic
NR4A2
(S110fs +1 more)
Duplication
(frameshift variant)
Epilepsy
GLikely pathogenic
NR4A2
(H103R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NR4A2
(M34V +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
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