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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC101927178, PPP2R3C
(L103P)
Single nucleotide variant
(5 prime UTR variant +2 more)
Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
GPathogenic
LOC101927178, PPP2R3C
(L193S +1 more)
Single nucleotide variant
(missense variant +1 more)
Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
GPathogenic
LOC101927178, PPP2R3C
(F350S +1 more)
Single nucleotide variant
(missense variant +1 more)
Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy
GPathogenic
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