ClinVar Miner

List of variants in gene SI 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_001041.4(SI):c.517C>G (p.Pro173Ala)	rs146960446	0.01286
NM_001041.4(SI):c.598A>G (p.Ser200Gly)	rs113903766	0.01139

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