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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992055, TNIP2
(R145C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC129992055, TNIP2
(V35I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
LOC129992055, TNIP2
(D141N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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