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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTPRC
(S42I)
Single nucleotide variant
(missense variant +1 more)
Immunodeficiency 104
GUncertain significance
PTPRC
(T332I +1 more)
Single nucleotide variant
(missense variant)
Immunodeficiency 104
GUncertain significance
PTPRC
(L830F +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
PTPRC
Single nucleotide variant
(intron variant)
Immunodeficiency 104
GLikely benign
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