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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SDCCAG8
(Q509E +3 more)
Single nucleotide variant
(missense variant)
Bardet-Biedl syndrome 16
+2 more
GUncertain significance
SDCCAG8
(E434K +3 more)
Single nucleotide variant
(missense variant)
Bardet-Biedl syndrome 16
+1 more
GUncertain significance
SDCCAG8
(R694K +3 more)
Single nucleotide variant
(missense variant)
Bardet-Biedl syndrome 16
GUncertain significance
ADSS2, AKT3
+13 more
Copy number loss
not provided
GPathogenic
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