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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SHOX2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
SHOX2
(M99L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SHOX2
Duplication
(inframe_insertion)
not specified
GLikely benign
SHOX2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
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