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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF11
(R312*)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic/Likely pathogenic
KIF11
(V627I)
Single nucleotide variant
(missense variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GUncertain significance
KIF11
(G790A)
Single nucleotide variant
(missense variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GUncertain significance
KIF11
(I902V)
Single nucleotide variant
(missense variant)
Microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
GUncertain significance
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