List of variants reported as benign for Familial Mediterranean fever by Women's Health and Genetics/Laboratory Corporation of America, 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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000243.3(MEFV):c.942C>T (p.Arg314=)	rs224213	0.61317
NM_000243.3(MEFV):c.1530T>C (p.Asp510=)	rs224206	0.59561
NM_000243.3(MEFV):c.1422G>A (p.Glu474=)	rs224208	0.57768
NM_000243.3(MEFV):c.306T>C (p.Asp102=)	rs224225	0.48544
NM_000243.3(MEFV):c.495C>A (p.Ala165=)	rs224223	0.48450
NM_000243.3(MEFV):c.1764G>A (p.Pro588=)	rs1231122	0.41230
NM_000243.3(MEFV):c.605G>A (p.Arg202Gln)	rs224222	0.20976
NM_000243.3(MEFV):c.1503C>T (p.Arg501=)	rs76464258	0.00733
NM_000243.3(MEFV):c.1759+8C>T	rs77380520	0.00321
NM_000243.3(MEFV):c.414A>G (p.Gly138=)	rs224224

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.