List of variants in gene OTOG reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001292063.2(OTOG):c.3096C>T (p.Asn1032=)	rs75133799	0.00891
NM_001292063.2(OTOG):c.4606C>T (p.Leu1536Phe)	rs117380920	0.00806
NM_001292063.2(OTOG):c.5235C>A (p.Leu1745=)	rs193083374	0.00701
NM_001292063.2(OTOG):c.2098G>A (p.Ala700Thr)	rs113745835	0.00467
NM_001292063.2(OTOG):c.8476C>T (p.Arg2826Cys)	rs191662816	0.00208

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