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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASP8
(I144M +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+2 more
GUncertain significance
CASP8
(R7S)
Single nucleotide variant
(synonymous variant +5 more)
CASP8-related disorder
GLikely benign
CASP8
Single nucleotide variant
(synonymous variant +2 more)
CASP8-related disorder
GLikely benign
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