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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED13
(M1895fs)
Deletion
(frameshift variant)
Intellectual developmental disorder 61
+1 more
GPathogenic/Likely pathogenic
MED13
(G1441A)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
MED13
(R1222H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
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