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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KNL1
(M151V +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 4, primary, autosomal recessive
+1 more
GBenign/Likely benign
KNL1
(I698L +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
KNL1
(I2038V +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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