List of variants reported as likely benign for Multiple endocrine neoplasia, type 1 by Myriad Genetics, Inc.

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.512G>A (p.Arg171Gln)	rs607969	0.01309
NM_001370259.2(MEN1):c.-20G>A	rs386134244	0.00158
NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp)	rs375804228	0.00015
NM_001370259.2(MEN1):c.1506G>C (p.Lys502Asn)	rs774296730	0.00014
NM_001370259.2(MEN1):c.1535C>T (p.Ser512Leu)	rs141679530	0.00011
NM_001370259.2(MEN1):c.511C>T (p.Arg171Trp)	rs143329068	0.00009
NM_001370259.2(MEN1):c.655-4del	rs748005956	0.00009
NM_001370259.2(MEN1):c.1391C>T (p.Ala464Val)	rs778728934	0.00007
NM_001370259.2(MEN1):c.1098A>T (p.Glu366Asp)	rs149383809	0.00004
NM_001370259.2(MEN1):c.1350+6G>A	rs746077651	0.00002
NM_001370259.2(MEN1):c.784-16C>T	rs754257177	0.00002
NM_001370259.2(MEN1):c.1350+3G>A
NM_001370259.2(MEN1):c.61C>A (p.Arg21Ser)	rs541476418

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.