Variants with conflicting interpretations "benign" from H3Africa Consortium and "likely benign" from any submitter

Minimum review status of the submission from H3Africa Consortium:		Collection method of the submission from H3Africa Consortium:
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: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001308093.3(GATA4):c.617-113T>C	rs3735819	0.80128
NM_002843.4(PTPRJ):c.827A>C (p.Gln276Pro)	rs1566734	0.14574
NM_001174096.2(ZEB1):c.233A>C (p.Asn78Thr)	rs80194531	0.01629
NM_000483.5(APOC2):c.229A>C (p.Lys77Gln)	rs5126	0.00784
NM_000041.4(APOE):c.487C>T (p.Arg163Cys)	rs769455	0.00701
NM_002875.5(RAD51):c.449G>A (p.Arg150Gln)	rs121917739	0.00171

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.