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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAPRE2
(A111T +3 more)
Single nucleotide variant
(missense variant +1 more)
Skin creases, congenital symmetric circumferential, 2
GUncertain significance
MAPRE2
(R143C +3 more)
Single nucleotide variant
(missense variant +1 more)
Developmental disorder
+1 more
GPathogenic/Likely pathogenic
MAPRE2
(R120Q +3 more)
Single nucleotide variant
(missense variant +1 more)
Skin creases, congenital symmetric circumferential, 2
GLikely pathogenic
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