Variants with conflicting interpretations "likely benign" from GeneDx and "risk factor" from any submitter

Minimum review status of the submission from GeneDx:		Collection method of the submission from GeneDx:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000796.6(DRD3):c.25G>A (p.Gly9Ser)	rs6280	0.53929
NM_004132.5(HABP2):c.1601G>A (p.Gly534Glu)	rs7080536	0.02383
NM_000514.4(GDNF):c.448G>A (p.Asp150Asn)	rs76466003	0.00230
NM_021175.4(HAMP):c.212G>A (p.Gly71Asp)	rs104894696	0.00197
NM_207034.3(EDN3):c.670G>A (p.Ala224Thr)	rs11570351	0.00164
NM_002485.5(NBN):c.511A>G (p.Ile171Val)	rs61754966	0.00145
NM_014946.4(SPAST):c.134C>A (p.Pro45Gln)	rs121908517	0.00063
NM_000249.4(MLH1):c.394G>C (p.Asp132His)	rs28930073	0.00019
NM_021912.5(GABRB3):c.44C>T (p.Ser15Phe)	rs121913126	0.00016

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.