List of variants in gene OTC reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000531.6(OTC):c.*175T>C	rs752290309	0.00015
NM_000531.6(OTC):c.*105C>T	rs1036076773	0.00012
NM_000531.6(OTC):c.*276A>G	rs1016109235	0.00003
NM_000531.6(OTC):c.76C>T (p.Arg26Trp)	rs1057515879	0.00002
NM_000531.6(OTC):c.896C>T (p.Thr299Ile)	rs756772340	0.00001
NM_000531.6(OTC):c.216+10A>G	rs1473033144
NM_000531.6(OTC):c.814G>A (p.Glu272Lys)	rs2068530106
NM_000531.6(OTC):c.974C>T (p.Pro325Leu)	rs1602034625

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