List of variants in gene OTOF reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_194248.3(OTOF):c.2736G>C (p.Leu912=)	rs4335905	0.56927
NM_194248.3(OTOF):c.158C>T (p.Ala53Val)	rs1879761	0.02762
NM_194248.3(OTOF):c.1926C>T (p.Asn642=)	rs72853741	0.02727
NM_194248.3(OTOF):c.3189G>A (p.Ala1063=)	rs80356573	0.01570
NM_194248.3(OTOF):c.2317C>T (p.Arg773Cys)	rs80356569	0.01549
NM_194248.3(OTOF):c.3247G>C (p.Ala1083Pro)	rs80356574	0.01529
NM_194248.3(OTOF):c.2464C>T (p.Arg822Trp)	rs80356570	0.01518
NM_194248.3(OTOF):c.710+10C>T	rs55639868	0.00890
NM_194248.3(OTOF):c.1723G>A (p.Val575Met)	rs55676840	0.00781
NM_194248.3(OTOF):c.1185C>T (p.Thr395=)	rs61739877	0.00596
NM_194248.3(OTOF):c.3471G>T (p.Arg1157=)	rs61742191	0.00446
NM_194248.3(OTOF):c.4869C>T (p.Gly1623=)	rs61744000	0.00446
NM_194248.3(OTOF):c.4332C>T (p.Thr1444=)	rs149236286

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