List of variants in gene GJB2 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004004.6(GJB2):c.*1197T>A	rs11841182	0.04451
NM_004004.6(GJB2):c.-15C>T	rs72561725	0.01589
NM_004004.6(GJB2):c.457G>A (p.Val153Ile)	rs111033186	0.00247
NM_004004.6(GJB2):c.249C>G (p.Phe83Leu)	rs111033218	0.00150
NM_004004.6(GJB2):c.186C>T (p.Asn62=)	rs397516869	0.00016
NM_004004.6(GJB2):c.15G>A (p.Thr5=)	rs757226502	0.00001

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