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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STIL
(A744V +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 7, primary, autosomal recessive
GUncertain significance
STIL
(L167M +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 7, primary, autosomal recessive
GUncertain significance