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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARCN1
(E52G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
ARCN1
(E78del)
Microsatellite
(inframe_deletion +1 more)
Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
GLikely pathogenic
ARCN1
(E174fs +1 more)
Microsatellite
(frameshift variant)
Short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
GLikely pathogenic
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