ClinVar Miner

List of variants in gene BBS9 reported as uncertain significance by Revvity Omics, Revvity

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_198428.3(BBS9):c.2309A>G (p.Glu770Gly)	rs149668719	0.00013
NM_198428.3(BBS9):c.2527T>C (p.Cys843Arg)	rs2538378297

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