ClinVar Miner

Submissions for variant NM_001017922.1(ERMAP):c.139G>A (p.Glu47Lys)

gnomAD frequency: 0.00078 dbSNP: rs56047316

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

Download table as spreadsheet

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
OMIM	RCV000001995	SCV000022153	affects	Antigen in Scianna blood group system	2005-02-01	no assertion criteria provided	literature only

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.