ClinVar Miner

List of variants in gene OTOGL reported as not provided for Autosomal recessive nonsyndromic hearing loss 84B

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.1585C>T (p.Gln529Ter)	rs371465450	0.00007
GRCh37/hg19 12q21.31(chr12:80696112-80696398)x1
Single allele

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