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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BNC2
(H888R +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Lower urinary tract obstruction, congenital
+1 more
GPathogenic
BNC2
(R853*)
Single nucleotide variant
(nonsense +1 more)
Lower Urinary Tract Obstruction
+1 more
GPathogenic
LINC02201, LOC101927357
+6 more
Duplication
Lower urinary tract obstruction, congenital
GUncertain significance
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