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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STAG2
(E194fs)
Deletion
(frameshift variant)
not provided
GPathogenic
STAG2
Deletion
(splice acceptor variant)
not provided
GLikely pathogenic
STAG2
(D659N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
STAG2
(L1092H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
STAG2
(M1144V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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