List of variants in gene GJB2 reported as uncertain significance for Hearing loss

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: 4

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HGVS	dbSNP
NM_004004.6(GJB2):c.101T>C (p.Met34Thr)	rs35887622
NM_004004.6(GJB2):c.226C>G (p.Leu76Val)	rs1566528748
NM_004004.6(GJB2):c.355G>A (p.Glu119Lys)	rs150529554
NM_004004.6(GJB2):c.560A>G (p.Glu187Gly)	rs1451982228

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