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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADM
(I233T +4 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
MPDZ
(Q1432* +4 more)
Single nucleotide variant
(nonsense)
Hydrocephalus, nonsyndromic, autosomal recessive 2
GLikely pathogenic
MPDZ
(G1272R +3 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
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