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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED25
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MED25
Single nucleotide variant
(intron variant)
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome
+4 more
GBenign