Variants with conflicting interpretations "other" from Eurofins NTD LLC (GA) and "drug response" from PharmGKB

Minimum review status of the submission from Eurofins NTD LLC (GA):		Collection method of the submission from Eurofins NTD LLC (GA):
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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024006.4(VKORC1):c.-1639G>A	rs9923231	0.31157
NM_005957.5(MTHFR):c.665C>T (p.Ala222Val)	rs1801133	0.27446
NM_006446.5(SLCO1B1):c.521T>C (p.Val174Ala)	rs4149056	0.12106
NM_000041.2(APOE):c.526C>T (p.Arg176Cys)	rs7412	0.07986

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.