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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SZT2-AS1, SZT2
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GLikely benign
SZT2, SZT2-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
+2 more
GBenign/Likely benign