List of variants in gene OTOGL reported as uncertain significance for auditory system disorder

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001378609.3(OTOGL):c.3488A>G (p.Asp1163Gly)	rs202085918	0.00195
NM_001378609.3(OTOGL):c.2564C>T (p.Pro855Leu)	rs183159689	0.00111
NM_001378609.3(OTOGL):c.475C>T (p.Arg159Trp)	rs191608225	0.00041
NM_001378609.3(OTOGL):c.1395-3T>C	rs374833540	0.00038
NM_001378609.3(OTOGL):c.3566A>G (p.Gln1189Arg)	rs200392453	0.00029
NM_001378609.3(OTOGL):c.6864A>G (p.Ile2288Met)	rs145876584	0.00029
NM_001378609.3(OTOGL):c.34C>A (p.Pro12Thr)	rs539100194	0.00015
NM_001378609.3(OTOGL):c.5350G>A (p.Val1784Met)	rs571909899	0.00015
NM_001378609.3(OTOGL):c.236-2A>G	rs766564988	0.00009
NM_001378609.3(OTOGL):c.2945A>C (p.Asp982Ala)	rs774797627	0.00006
NM_001378609.3(OTOGL):c.3434C>T (p.Ala1145Val)	rs374368341	0.00006
NM_001378609.3(OTOGL):c.890T>G (p.Val297Gly)	rs776891390	0.00003
NM_001378609.3(OTOGL):c.4234A>G (p.Met1412Val)	rs774172292	0.00002
NM_001378609.3(OTOGL):c.4544G>A (p.Arg1515Gln)	rs201232946	0.00002
NM_001378609.3(OTOGL):c.5050G>A (p.Gly1684Arg)	rs778223464	0.00002
NM_001378609.3(OTOGL):c.1892C>A (p.Ser631Tyr)	rs373638514	0.00001
NM_001378609.3(OTOGL):c.2854G>A (p.Gly952Arg)	rs759133667	0.00001
NM_001378609.3(OTOGL):c.3277A>C (p.Asn1093His)	rs867315415	0.00001
NM_001378609.3(OTOGL):c.3931C>T (p.His1311Tyr)	rs1230531336	0.00001
NM_001378609.3(OTOGL):c.4231A>T (p.Asn1411Tyr)	rs770438244	0.00001
NM_001378609.3(OTOGL):c.1694A>G (p.Gln565Arg)
NM_001378609.3(OTOGL):c.3626A>G (p.Tyr1209Cys)	rs1886838397
NM_001378609.3(OTOGL):c.6161G>A (p.Cys2054Tyr)	rs962629988
NM_001378609.3(OTOGL):c.6235T>C (p.Cys2079Arg)
NM_001378609.3(OTOGL):c.6949T>C (p.Cys2317Arg)	rs1197672891

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