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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DONSON
(F165S)
Single nucleotide variant
(missense variant)
Meier-Gorlin syndrome
+1 more
GPathogenic/Likely pathogenic
DONSON
(L49fs)
Duplication
(frameshift variant)
Microcephaly, short stature, and limb abnormalities
GPathogenic