List of variants reported as benign for vertebral column disorder by Labcorp Genetics (formerly Invitae), Labcorp

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001040167.2(LFNG):c.482-4A>G	rs62444250	0.05791
NM_001040167.2(LFNG):c.972G>A (p.Ser324=)	rs12700028	0.04179
NM_001040167.2(LFNG):c.1002C>T (p.Tyr334=)	rs61743870	0.03693
NM_001040167.2(LFNG):c.481+3G>A	rs141008352	0.00361
NM_001040167.2(LFNG):c.75C>T (p.Thr25=)	rs767338996	0.00209
NM_001040167.2(LFNG):c.612C>T (p.Tyr204=)	rs147266260	0.00105
NM_001040167.2(LFNG):c.581+14C>T	rs371327031	0.00061
NM_001040167.2(LFNG):c.920G>A (p.Arg307His)	rs201791522	0.00021
NM_001040167.2(LFNG):c.988-12C>T	rs200232463	0.00019
NM_001040167.2(LFNG):c.822-9C>G	rs199661195	0.00017
NM_001040167.2(LFNG):c.1074-16T>C	rs143421936	0.00011
NM_001040167.2(LFNG):c.988-16C>T	rs376736772	0.00002
NM_001040167.2(LFNG):c.1104G>A (p.Pro368=)	rs544123371

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.