ClinVar Miner

List of variants in gene GJB2 reported as likely benign by EGL Genetic Diagnostics, Eurofins Clinical Diagnostics

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
NM_004004.6(GJB2):c.*3C>A	rs111033460
NM_004004.6(GJB2):c.11G>A (p.Gly4Asp)	rs111033222
NM_004004.6(GJB2):c.368C>A (p.Thr123Asn)	rs111033188

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