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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STIL
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
STIL
Single nucleotide variant
(synonymous variant)
Microcephaly 7, primary, autosomal recessive
+2 more
GBenign
STIL
(A86V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
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