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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC108281134, SOX3
(P64del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GConflicting classifications of pathogenicity
LOC108281134, SOX3
(L50P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC108281134, SOX3
(S23T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC108281134, SOX3
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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