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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
IMP3, LOC130057619
(C98W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
IMP3, LOC130057619
(P90L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance