List of variants in gene SDCCAG8 reported as pathogenic for Bardet-Biedl syndrome

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006642.5(SDCCAG8):c.696T>G (p.Tyr232Ter)	rs772544112	0.00006
NM_006642.5(SDCCAG8):c.740+356C>T	rs397515337	0.00006
NM_006642.5(SDCCAG8):c.1717C>T (p.Gln573Ter)	rs1286714661	0.00001
NM_006642.5(SDCCAG8):c.1420del (p.Glu474fs)	rs397515335

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