List of variants reported as uncertain significance for endocrine gland neoplasm by Institute of Human Genetics, University of Leipzig Medical Center

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys)	rs773500082	0.00006
NM_017841.4(SDHAF2):c.352A>G (p.Ile118Val)	rs747994812	0.00001
NM_001370259.2(MEN1):c.1003C>T (p.Arg335Trp)	rs371364206
NM_001370259.2(MEN1):c.1185+1G>A	rs1941661315
NM_001370259.2(MEN1):c.1780A>G (p.Thr594Ala)	rs1941488490
NM_020975.6(RET):c.1934_1936del (p.Ser645del)	rs1416677590
NM_024529.5(CDC73):c.192TAA[1] (p.Asn66del)

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.