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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INPP5K
(P189S +1 more)
Single nucleotide variant
(missense variant)
Congenital muscular dystrophy with cataracts and intellectual disability
GUncertain significance
INPP5K
(G140D +1 more)
Single nucleotide variant
(missense variant)
Congenital muscular dystrophy with cataracts and intellectual disability
GUncertain significance