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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC6A5
(C3*)
Single nucleotide variant
(5 prime UTR variant +1 more)
Hyperekplexia 3
+1 more
GPathogenic/Likely pathogenic
SLC6A5
Single nucleotide variant
(5 prime UTR variant +1 more)
Hyperekplexia 3
+2 more
GBenign/Likely benign