List of variants in gene BBS10 reported as likely pathogenic for retinal disorder

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_024685.4(BBS10):c.206T>A (p.Val69Glu)	rs1176176320	0.00001
NM_024685.4(BBS10):c.590A>G (p.Tyr197Cys)	rs756632517

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