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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MPDZ
(A1760T +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MPDZ
(L501fs)
Duplication
(frameshift variant)
not provided
GPathogenic
MPDZ
(Q210*)
Single nucleotide variant
(nonsense)
Hydrocephalus, nonsyndromic, autosomal recessive 2
GPathogenic
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