ClinVar Miner

List of variants in gene BBS12 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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_152618.3(BBS12):c.116T>C (p.Ile39Thr)	rs138036823	0.00577
NM_152618.3(BBS12):c.1103G>A (p.Arg368His)	rs78457123	0.00511

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