List of variants in gene OTOG reported as likely benign by Eurofins NTD LLC (GA)

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001292063.2(OTOG):c.8542-8C>T	rs182750732	0.00565
NM_001292063.2(OTOG):c.7631G>A (p.Arg2544Gln)	rs76461792	0.00308
NM_001292063.2(OTOG):c.2398G>A (p.Asp800Asn)	rs141010212	0.00287
NM_001292063.2(OTOG):c.6074C>T (p.Ala2025Val)	rs61736002	0.00229
NM_001292063.2(OTOG):c.7650C>T (p.Ile2550=)	rs187445787	0.00200
NM_001292063.2(OTOG):c.1285C>T (p.Arg429Trp)	rs199968574	0.00166
NM_001292063.2(OTOG):c.4627G>A (p.Ala1543Thr)	rs545740473	0.00067

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