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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED25
Single nucleotide variant
(synonymous variant)
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome
+2 more
GLikely benign
MED25
(L480V)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
MED25
Single nucleotide variant
(intron variant)
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome
+4 more
GBenign/Likely benign
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