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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EGR3
(G367S +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
EGR3
(P146T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
EGR3
(Y32F +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
EGR3
(D41E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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