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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RTTN
(A1476S +1 more)
Single nucleotide variant
(missense variant)
Microcephalic primordial dwarfism due to RTTN deficiency
GUncertain significance
RTTN
(P752R)
Single nucleotide variant
(5 prime UTR variant +1 more)
Microcephalic primordial dwarfism due to RTTN deficiency
GUncertain significance
RTTN
(E640*)
Single nucleotide variant
(5 prime UTR variant +1 more)
Microcephalic primordial dwarfism due to RTTN deficiency
GLikely pathogenic
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