List of variants in gene OTOG reported as likely benign for autosomal recessive nonsyndromic hearing loss 18B

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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	gnomAD frequency
NM_001292063.2(OTOG):c.4238G>A (p.Arg1413Gln)	rs143848095	0.00260
NM_001292063.2(OTOG):c.6827C>T (p.Thr2276Ile)	rs569603083	0.00078
NM_001292063.2(OTOG):c.4002C>T (p.Phe1334=)	rs545896255	0.00032
NM_001292063.2(OTOG):c.7464C>T (p.Cys2488=)	rs774023506	0.00003

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