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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIB1
(C112F)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 7
GUncertain significance
MIB1
(N762S)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 7
GUncertain significance
MIB1
(I1003V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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