List of variants in gene GJB2 reported as 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: 10

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HGVS	dbSNP
NM_004004.6(GJB2):c.-15C>T	rs72561725
NM_004004.6(GJB2):c.-22-12C>T	rs9578260
NM_004004.6(GJB2):c.-6T>A	rs148136545
NM_004004.6(GJB2):c.249C>G (p.Phe83Leu)	rs111033218
NM_004004.6(GJB2):c.341A>G (p.Glu114Gly)	rs2274083
NM_004004.6(GJB2):c.380G>A (p.Arg127His)	rs111033196
NM_004004.6(GJB2):c.457G>A (p.Val153Ile)	rs111033186
NM_004004.6(GJB2):c.478G>A (p.Gly160Ser)	rs34988750
NM_004004.6(GJB2):c.608T>C (p.Ile203Thr)	rs76838169
NM_004004.6(GJB2):c.79G>A (p.Val27Ile)	rs2274084

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