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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
B9D1
Single nucleotide variant
(splice donor variant)
Joubert syndrome 27
+3 more
GPathogenic/Likely pathogenic
B9D1, LOC130060455
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign