List of variants reported as benign for Ornithine aminotransferase deficiency by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000274.3(OAT):c.-94T>G	rs4144117	0.82728
NM_000274.4(OAT):c.648+14A>G	rs9422807	0.81973
NM_000274.4(OAT):c.1134C>T (p.Asn378=)	rs11461	0.33660
NM_000274.4(OAT):c.*185C>T	rs2459216	0.10300
NM_000274.4(OAT):c.*535T>C	rs8182	0.06407
NM_000274.4(OAT):c.-53C>T	rs117824913	0.01420
NM_000274.4(OAT):c.200-10T>C	rs80313473	0.00780
NM_000274.4(OAT):c.-38C>T	rs9422945	0.00489
NM_000274.4(OAT):c.-59G>C	rs144950523

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.