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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130004949, PTPRE
(P58L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC130004949, PTPRE
(P39L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC130004949, PTPRE
(P66L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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