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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KNL1
(K846N +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 4, primary, autosomal recessive
GUncertain significance
KNL1
(M965L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance