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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYCR2
(Q152H +1 more)
Single nucleotide variant
(missense variant)
Hypomyelinating leukodystrophy 10
GUncertain significance
PYCR2
Single nucleotide variant
(intron variant)
Hypomyelinating leukodystrophy 10
GUncertain significance