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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CMIP, LOC130059505
(A92T)
Single nucleotide variant
(missense variant)
CMIP-related disorder
GUncertain significance
CMIP, LOC130059505
Deletion
(splice donor variant)
CMIP-related disorder
GUncertain significance