List of variants in gene GJB2 reported as pathogenic for Nonsyndromic Deafness

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.109G>A (p.Val37Ile)	rs72474224
NM_004004.6(GJB2):c.238C>T (p.Gln80Ter)	rs199883710
NM_004004.6(GJB2):c.269dup (p.Val91fs)	rs730880338

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