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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KIF14
Single nucleotide variant
(synonymous variant)
Microcephaly 20, primary, autosomal recessive
+2 more
GBenign/Likely benign
KIF14
(V363I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+4 more
GLikely benign