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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF14
(R1046C +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 20, primary, autosomal recessive
GUncertain significance
KIF14
(E337K)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+2 more
GUncertain significance