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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GEMIN4
(W818R)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
GLikely pathogenic
GEMIN4
(S755F)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
+1 more
GUncertain significance
GEMIN4
(P596L)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
GUncertain significance
GEMIN4
(Q225*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
GUncertain significance
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