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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC107652445, SHOX
(K116fs)
Deletion
(frameshift variant)
Connective tissue disorder
GLikely pathogenic
LOC107652445, SHOX
Single nucleotide variant
(synonymous variant)
SHOX-related short stature
+2 more
GBenign/Likely benign