List of variants in gene GJB2 reported as uncertain significance by Fulgent Genetics,Fulgent Genetics

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.188T>C (p.Val63Ala)	rs727504309
NM_004004.6(GJB2):c.663G>C (p.Lys221Asn)	rs375599392
NM_004004.6(GJB2):c.670A>C (p.Lys224Gln)	rs111033194

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