List of variants in gene BBS9 reported as likely pathogenic for not provided

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_198428.3(BBS9):c.1561C>T (p.Arg521Ter)	rs748601675	0.00001
NM_198428.3(BBS9):c.832C>T (p.Arg278Ter)	rs767005321	0.00001
NM_198428.3(BBS9):c.1283_1286del (p.Thr428fs)
NM_198428.3(BBS9):c.263C>A (p.Ser88Ter)	rs749974697
NM_198428.3(BBS9):c.658C>T (p.Gln220Ter)

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