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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BBS10
(V319L)
Single nucleotide variant
(missense variant)
Bardet-Biedl syndrome 10
GUncertain significance
BBS10
(T79fs)
Deletion
(frameshift variant)
Bardet-Biedl syndrome 10
+1 more
GPathogenic/Likely pathogenic
BBS10
Single nucleotide variant
(synonymous variant)
Bardet-Biedl syndrome
+1 more
GConflicting classifications of pathogenicity
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