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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYCR2
(R266* +1 more)
Single nucleotide variant
(nonsense)
Hypomyelinating leukodystrophy 10
+1 more
GPathogenic
PYCR2
(A14P)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity