ClinVar Miner

List of variants in gene GJB6 reported as likely 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001110219.3(GJB6):c.322C>T (p.Arg108Ter)	rs772862268	0.00003
NM_001110219.3(GJB6):c.487del (p.Leu163fs)	rs1566538321

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