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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC39A4
(L125P +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
LOC130001397, SLC39A4
(G14W +3 more)
Single nucleotide variant
(missense variant)
Hereditary acrodermatitis enteropathica
GUncertain significance
SLC39A4
(P108fs +2 more)
Deletion
(frameshift variant)
Hereditary acrodermatitis enteropathica
GLikely pathogenic
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