List of variants in gene combination AKT3, SDCCAG8 reported as uncertain significance for Bardet-Biedl syndrome 16

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006642.5(SDCCAG8):c.2067G>A (p.Leu689=)	rs191821211	0.00038
NM_006642.5(SDCCAG8):c.*149T>C	rs1057515424
NM_006642.5(SDCCAG8):c.*97G>A	rs554190542

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