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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPEG, ASIC4-AS1
(I2324N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
DNM2
(R66Q)
Single nucleotide variant
(missense variant)
Fetal akinesia-cerebral and retinal hemorrhage syndrome
+2 more
GUncertain significance
DNM2
(I232T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
DNM2
(R465W)
Single nucleotide variant
(missense variant)
Centronuclear myopathy
GPathogenic
DNM2
(H727Y +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
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