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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RTTN
(R1591Q +1 more)
Single nucleotide variant
(missense variant)
Microcephalic primordial dwarfism due to RTTN deficiency
+2 more
GUncertain significance
RTTN
(M435I)
Single nucleotide variant
(5 prime UTR variant +1 more)
Microcephalic primordial dwarfism due to RTTN deficiency
+1 more
GConflicting classifications of pathogenicity
RTTN
(L267V)
Single nucleotide variant
(5 prime UTR variant +1 more)
Microcephalic primordial dwarfism due to RTTN deficiency
+1 more
GUncertain significance
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