List of variants in gene combination BBS1, ZDHHC24 reported as likely benign 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024649.5(BBS1):c.1194C>A (p.Ile398=)	rs200577824	0.00023
NM_024649.5(BBS1):c.1320A>G (p.Arg440=)	rs1430151544	0.00001
NM_024649.5(BBS1):c.1578G>A (p.Ala526=)	rs373397428	0.00001

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