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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MPDZ
(R2026Q +7 more)
Single nucleotide variant
(missense variant)
Hydrocephalus, nonsyndromic, autosomal recessive 2
+1 more
GBenign/Likely benign
MPDZ
(D123N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance