ClinVar Miner

List of variants in gene SGCB reported as likely benign by Genetics and Genomics Program, Sidra Medicine

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_000232.5(SGCB):c.794C>T (p.Thr265Ile)	rs116214830	0.00025
NM_000232.5(SGCB):c.368A>C (p.Tyr123Ser)	rs398123263

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